Trauma Injury

30

Review clinical trials related to Trauma Injury. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Therapy Dog Visits for Patients Hospitalized With Traumatic Injuries

Animal assisted therapy (AAT) with dogs has been shown to be beneficial for a wide range of patients with both acute and chronic illnesses, including spinal cord injuries, heart failure, myocardial infarctions, strokes, cancer, post-traumatic stress disorder, and depression. Studies have also demonstrated that even in healthy adults, the presence of dogs is associated with physiologic changes such as increased pain threshold, decreased blood pressure, and decreased heart rate. However, few studies have investigated the role of AAT in the post-operative course in adults. This study will investigate the impact of therapy dog visits on pain and anxiety scores for trauma patients at Boston Medical Center (BMC).

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Boston Medical CenterUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Patients admitted to the Trauma and Acute Care Surgery (TACS) service following... [+2]

Fear of dogs, allergy to dogs [+3]

Status: Not yet recruiting

Self-directed Mobile Mindfulness to Address ICU Survivors' Psychological Distress

Serious acute heart and lung illnesses like heart failure, severe COVID, and sepsis often leave survivors struggling not only physically, but also with lasting depression, anxiety, and stress. These problems that are hard to treat because access to mental health care is often limited. To help address this, the researchers created Lift, a fully automated mindfulness program designed with patient input and delivered through a mobile app. The investigators now plan a large, multi-site study to test whether Lift improves mental health and quality of life over six months compared to a critical illness education program called Enlighten Recovery. Overall the goal is to make an easy-to-use, widely accessible program available to people across the U.S., including those who speak Spanish.

Participants needed: 450
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Duke UniversityUpdated: Jun 16, 2026Locations: 3
Eligibility criteria

Adult (age ≥18) [+14]

Severe psychological distress as assessed by endorsement of active suicidality (... [+2]

Status: Recruiting

Mortality of Trauma in the Intensive Care Unit.

In this study, it was planned to establish the factors associated with severe trauma discharged from the intensive care unit and mortality. A cross-sectional trial will be conducted to review the ICU discharge database at a two-year interval to review records of trauma admissions patients and compare them with other types of admissions. Participant institutions are general hospitals (public and private) from the Colombian Orinoco region. the prevalence of admission by trauma will also be determined.

Participants needed: 500
Trial details
Age: 15-100Biological sex: AllType: ObservationalSponsor: Hospital Departamental de VillavicencioUpdated: May 27, 2026Locations: 1
Eligibility criteria

Admitted to the intensive care unit.

None.

Status: Recruiting

Patient Experience of Older Adults Living Alone With Injuries

This study aims to explore the patient experiences of living alone older adults with injuries, and to examine the effects of a "Geriatric Trauma Care Program" in older adults with limb injuries who live alone. A three-year design will be used to reach the purposes of this study. The first stage of this study will use descriptive phenomenology to get patient experiences of living alone older adults with injuries. In the second stage of this study, a two-arm experimental design will be used.

Participants needed: 110
Trial details
Age: 65-74Biological sex: AllType: InterventionalSponsor: Kaohsiung Medical University Chung-Ho Memorial HospitalUpdated: May 27, 2026Locations: 2
Eligibility criteria

willing to join this study for 12 weeks [+6]

with an ISS greater than 16 (severe injuries) [+3]

Status: Recruiting

Massive Transfusion in Children-2: A Trial Examining Life Threatening Hemorrhage in Children

The MATIC-2 is a multicenter clinical trial enrolling children who are less than 18 years of age with hemorrhagic shock potentially needing significant blood transfusion. The primary objective of the clinical trial is to determine the effectiveness of Low Titer Group O Whole Blood (LTOWB) compared to component therapy (CT), and Tranexamic Acid (TXA) compared to placebo in decreasing 24-hour all-cause mortality in children with traumatic life threatening hemorrhage.

Participants needed: 1,000
Trial details
Phase: Phase 3Age: Up to 17Biological sex: AllType: InterventionalSponsor: Philip SpinellaUpdated: May 11, 2026Locations: 23
Eligibility criteria

Children, defined as less than estimated18 years of age with traumatic injury [+4]

Patient with devastating traumatic brain injury not expected to survive due to m... [+12]

Status: Not yet recruiting

Human-centered Injury Thrivorship Pathway for Survivors of Physical Trauma

The goal of this clinical trial is to pilot and evaluate a human-centered injury thrivorship pathway in injury survivors. The main question it aims to answer is: • Is the pathway appropriate, acceptable, and feasible to meet the medical and social needs of injury survivors? Injury survivors will be purposively sampled to enroll in the pathway and asked to participate in in-depth interviews and their use of pathway resources will be tracked.

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: May 1, 2026Locations: 1
Eligibility criteria

Patient ≥ 18 years old presenting with a physical injury to Zuckerberg San Franc... [+4]

Patient < 18 years old [+2]

Status: Not yet recruiting

Bioengineered Penile Tissue Constructs for Irreversibly Damaged Penile Corpora

The primary objective of this clinical trial is to evaluate the safety of autologous engineered corpora cavernosa + albuginea constructs for treatment of complex penile deformities. Autologous endothelial and smooth muscle cells obtained from enrolled subjects' corpora cavernosa biopsy sample, will be culture expanded in vitro and used to seed decellularized corpora cavernosa + albuginea obtained from cadaveric-donors to create autologous bioengineered corpora cavernosa/albuginea constructs for repair of damaged penile tissues.

Participants needed: 10
Trial details
Phase: Phase 1Age: 18-60Biological sex: MaleType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Males aged 18-60 years. [+7]

Presence of untreated or incompletely treated urinary tract infection at the tim... [+21]

Status: Recruiting

Study of ICG Fluorescence Imaging in Open Fracture and Infection Patients

The purpose of this study is to determine whether an indocyanine green (ICG) fluorescence imaging system (cBPI) can be used to provide surgeons with information about bone health or bone blood flow. This will help surgeons better understand the healing potential of bone and relative risk of complication. This is important to help surgeons select the most appropriate treatment for severe traumatic injuries and infections.

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dartmouth-Hitchcock Medical CenterUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Patients 18 years of age or older. [+4]

Inability of patient to provide informed consent [+3]

Status: Recruiting

The Role of Brain-Bone Marrow-Gut Interaction Following Major Trauma

Traumatic injury followed by critical illness provokes pathophysiologic changes in the bone marrow and the gut that contribute to persistent anemia and changes in the microbiome which significantly impact long-term recovery. This project will define the interactions between the stress, chronic inflammation, bone marrow dysfunction, and an altered microbiome which will provide a strong foundation for future clinical interventions to help improve outcomes following severe trauma.

Participants needed: 275
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of FloridaUpdated: Feb 6, 2026Locations: 3
Eligibility criteria

All adults (age ≥18). [+2]

Patients not expected to survive greater than 48 hours [+18]

Status: Not yet recruiting

IV Injection of Metoclopramide With or Without Dexamethasone

Reflux and the aspiration of gastric contents have always been important focal points. Previous study stated that trauma is an important factor in aspiration pneumonia. Often, emergency trauma patients have residual gastric contents due to the ingestion of food before injury, the accidental swallowing of nasal and/or oral blood after injury, and delayed gastric emptying due to stress, pain, or the use of opioids. During sedation or general anesthesia, such satiated patients are often at risk of aspiration due to a reduction in lower esophageal sphincter tension and the protective inhibition of the airway reflex. Perioperative gastric ultrasound can be performed at a bedside ultrasound unit; it can safely, non-invasively, conveniently, and effectively evaluate the fullness of a patient's stomach and the nature of their gastric contents. It can also be used in the selection of an appropriate method for the anesthetic induction process and can reduce the risk of vomiting, aspiration, and related complications. As a gastric motility-promoting drug, metoclopramide can accelerate gastric emptying. Dexamethasone reduced the incidence of nausea and vomiting and improve gastric motility.

Participants needed: 1
Trial details
Phase: Early Phase 1Age: 16-50Biological sex: AllType: InterventionalSponsor: Ahmed Nassar Ibrahim MohammedUpdated: Jan 15, 2026
Eligibility criteria

Traumatic patients undergo emergency operations [+3]

A history of diseases of important organs, such as diabetes, gastro-paresis, liv... [+5]

Status: Recruiting

Hematopoietic Stem Cell Dysfunction in the Elderly After Severe Injury

Traumatic injury is a leading cause of morbidity and mortality in young adults, and remains a substantial economic and health care burden. Despite decades of promising preclinical and clinical investigations in trauma, investigators understanding of these entities is still incomplete, and few therapies have shown success. During severe trauma, bone marrow granulocyte stores are rapidly released into the peripheral circulation. This release subsequently induces the expansion and repopulation of empty or evacuated space by hematopoietic stem cells (HSCs). Although the patient experiences an early loss of bone marrow myeloid-derived cells, stem cell expansion is largely skewed towards the repopulation of the myeloid lineage/compartment. The hypothesis is that this 'emergency myelopoiesis' is critical for the survival of the severely traumatized and further, failure of the emergency myelopoietic response is associated with global immunosuppression and susceptibility to secondary infection. Also, identifying the release of myeloid derived suppressor cells (MDSCs) in the circulation of human severe trauma subjects. This process is driven by HSCs in the bone marrow of trauma subjects. Additionally, MDSCs may have a profound effect on the nutritional status of the host. The appearance of these MDSCs after trauma is associated with a loss of muscle tissue in these subjects. This muscle loss and possible increased catabolism have huge effects on long term outcomes for these subjects. It is the investigator's goal to understand the differences that occur in these in HSCs and muscle cells as opposed to non-injured and non-infected controls. This work will lead to a better understanding of the myelopoietic and catabolic response following trauma.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Jan 15, 2026Locations: 1
Eligibility criteria

All adults (age ≥18 to 54) [+7]

Patients not expected to survive greater than 48 hours. [+14]

Status: Recruiting

The Effects of Footplate Stiffness on Foot Loading Within Carbon Fiber Custom Dynamic Orthoses

Carbon fiber custom dynamic orthoses (CDOs) improve function, reduce pain, and offload the foot and ankle. CDOs include a proximal cuff that wraps around the leg just below the knee, a posterior carbon fiber strut that bends to store and return energy, and a semi-rigid carbon fiber footplate. The purpose of this study is to determine the effect of CDO use and CDO footplate stiffness on foot loading, limb mechanics, pain, and comfort.

Participants needed: 20
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Jason WilkenUpdated: Dec 31, 2025Locations: 1
Eligibility criteria

Between the ages of 18 and 65 [+5]

Diagnosed with a moderate or severe brain injury [+8]

Status: Recruiting

Pathological Myeloid Activation After Sepsis and Trauma

The goal of this observational study is to better understand what happens to circulating blood after a patient experiences severe trauma injury. The main questions it aims to answer are: Is severe human trauma associated with specific patterns of development in the hematopoietic stem cells of these patients? and Does the initial severe trauma injury create immunosuppression and increase risk of in-hospital sepsis? Participants in study will give blood samples and a waste sample of bone marrow at time of operative repair of traumatic orthopedic injuries, supply medical information and participate in surveys and assessments during recovery from their injury(ies). Researchers will compare severe trauma injury patients to elective hip repair patients to see if immunosuppression and specific development patterns occur in the trauma patient versus the otherwise healthy hip surgery patient.

Participants needed: 255
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of FloridaUpdated: Dec 26, 2025Locations: 1
Eligibility criteria

All adults age ≥ 18 years [+2]

Patients not expected to survive greater than 48 hours. [+21]

Status: Recruiting

Dysfunctional Myelopoiesis and Myeloid-Derived Suppressor Cells in Sepsis

Adverse outcomes in surgical sepsis patients are secondary to dysregulated emergency myelopoiesis, and expansion of myeloid-derived suppressor cells. Here we propose to determine the underlying mechanisms behind the increased expansion of these leukocyte populations and the underlying mechanisms that drive inflammation and immune suppression.

Participants needed: 450
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University of FloridaUpdated: Dec 26, 2025Locations: 1
Eligibility criteria

age ≥18 years [+1]

have disease states that predispose to significant immune system dysfunction [+16]

Status: Not yet recruiting

Assess the Efficacy of Tailored Patient Information and Voluntary Patient-managed Outpatient Digital Follow-up (I-POD) as an Adjunct to Standard Treatment According to National Guidelines in the National Trauma Plan Among Adult Trauma Patients in Norway.

The POSTRAUMA trial is a clinical trial at The Regional trauma centre of Western Norway, Haukeland University Hospital. Trauma is the leading cause of death worldwide in patients aged 1-45 years. In Norway, approximately 10,000 patients are admitted to hospital annually due to trauma, with 66% being male. The mean age is 43 years for male and 48 years for female, indicating a relatively young patient population. While mortality rates are decreasing, a significant proportion of trauma survivors experience long-term disabilities, reduced quality of life, and difficulties in returning to work. These consequences impose substantial burdens on individuals, families, and society. Considering these issues, a shift in focus is needed-from survival alone to long-term functional recovery and quality of life after trauma. Severe trauma often requires long-term follow-up, both physically and psychosocially. Traditional follow-up can be fragmented and not tailored to individual needs. Digital patient monitoring and tailored information have the potential to improve patient pathways, but knowledge about how these are experienced by patients is limited. The goal is to find out if Norwegian trauma patients who receive tailored patient information and patient-managed outpatient digital follow-up, in addition to standard treatment have: * Less disability * Return more often to work * Improved quality of life The study population are Norwegian trauma patients, 16 years or older at date of inclusion, who are admitted to Haukeland University hospital (HUS) following trauma with trauma team activation. 256 patients will be included in this trial. Participants will: * Answer a questionnaire at inclusion, one month, 6 months and 12 months. * Participants in the intervention group will be invited to digital outpatient follow up one month after the accident. * Some participants will be interviewed about how they experienced their trauma follow up.

Participants needed: 256
Trial details
Age: 16+Biological sex: AllType: InterventionalSponsor: Haukeland University HospitalUpdated: Dec 22, 2025Locations: 1
Eligibility criteria

16 years or older [+3]

15 years or younger [+7]

Status: Not yet recruiting

Traumatic Injury Clinical Trial Evaluating Tranexamic Acid in Children: An Efficacy Study

Trauma is the leading cause of death and disability in children in the United States. The objective of this study is to evaluate the benefits and harms of tranexamic acid (TXA; a drug that stops bleeding) in severely injured children with hemorrhagic brain and/or torso injuries. Using thromboelastography, we will measure baseline fibrinolysis to assess for treatment effects of TXA at different levels of fibrinolysis.

Participants needed: 2,000
Trial details
Phase: Phase 3Age: 0-17Biological sex: AllType: InterventionalSponsor: Daniel Nishijima, MD, MASUpdated: Dec 15, 2025
Eligibility criteria

Less than 18 years old AND [+12]

Unable to administer study drug within 3 hours of traumatic event [+15]

Status: Recruiting

UltrasouNd-guided Percutaneous Intercostal Nerve Cryoneurolysis for Analgesia Following Traumatic Rib Fracture

Traumatic rib fractures (i.e., broken ribs caused by a physical injury) are common and very painful. They also often lead to serious complications, more time spent in hospital, and can even lead to death. Even after rib fractures have healed, they can lead to long-term pain and a lower quality of life. A technology called cryoneurolysis, which acts to freeze nerves causing pain using a small tool which can turn very cold, is a promising new way to manage rib fracture pain. This study is a test with a small number of people to see if it is feasible to use this technology for patients with rib fractures. If this is successful, we will recruit more people for a larger study to see if cryoneurolysis, along with standard pain control techniques, is better at stopping pain, compared to just the normal techniques alone. Participants in our study will be asked to rate their pain, and record pain medications that they take for 3 months after their pain procedure.

Participants needed: 24
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: Sunnybrook Health Sciences CentreUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Aged ≥18 [+3]

Lack of patient consent; unlikely to comply with follow up [+9]

Status: Recruiting

RELIEVED (REgionaL anesthesIa PElVic fracturEs stuDy) Study. Regional Anesthesia (RA) Techniques for Pain Management in Pelvic Fractures: A Prospective, Monocentric, Pilot Cohort Study.

The goal of this observational clinical trial is to assess the impact of Regional Anesthesia (RA) techniques with the strongest anatomical and scientific support in controlling acute post-operative pain in pelvic/acetabular fractures, as well as their potential role in reducing complications related to excessive intra- and postoperative opioid use. The main questions it aims to answer are: Does RA lower opioid use in the first 24 hours after pelvic/acetabular fractures surgery? Does RA lower pain scores in the first 48 hours after surgery, incidence of complications and occurrence of persistent post-surgical pain? During the hours and days following surgery, the research team will evaluate and assess the intensity of any postoperative pain at predefined time points; quantify the use of pain medications and any related complications; and measure the possible onset of chronic pain and the timeline of functional recovery (through scheduled clinical follow-up at 30, 60, and 90 days). Participants will: at the time of surgery, and only in the presence of trained and certified anesthesiologists, patients will receive regional anesthesia techniques in addition to the standard multimodal analgesic treatment. In the absence of certified anesthesiologists, patients will be treated exclusively with systemic multimodal analgesia according to the standard protocol. All the procedures are part of the current clinical practice and no experimental techniques or medications are involved.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: A.O.U. Città della Salute e della ScienzaUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years and ability to provide informed consent [+1]

Age < 18 years [+1]

Status: Recruiting

OCT in Open Fracture and Infected Fracture

This is a pilot prospective, observational study of patients with open or infected fracture evaluating the feasibility and acceptability of OCT, a light-based imaging modality that requires no drug or contrast agent.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dartmouth-Hitchcock Medical CenterUpdated: Jun 27, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+2]

Metatarsal fractures

Status: Recruiting

Predictive Accuracy of PLR and PNR in Detecting ETIC

Observational study to know what is the predictive accuracy of platelet-neutrophil ratio (PNR) and platelet-lymphocyte ratio (PLR) done in patients presenting to ED( emergency department)within 6 hours of trauma; in detecting early trauma induced coagulopathy during hospital admission

Participants needed: 250
Trial details
Age: 12+Biological sex: AllType: ObservationalSponsor: Jubilee Mission Medical College and Research InstituteUpdated: Jul 2, 2025Locations: 1Duration: 1 Day
Eligibility criteria

All patients with trauma AND [+2]

Treated with intravenous fluids, drugs, whole blood and blood products elsewhere [+4]

Status: Recruiting

Bioimpedance for Ortho Trauma

Patients with high-energy extremity trauma will undergo imaging with an EIT device in the Emergency Department, Operating Room, Orthopaedic Clinic, and In-patient hospital rooms. The EIT device is an electrical impedance tomography system.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Dartmouth-Hitchcock Medical CenterUpdated: Jun 22, 2025Locations: 1
Eligibility criteria

Age 18 years or older [+2]

Metatarsal fractures [+3]

Status: Recruiting

Whole Blood in Trauma Patients With Hemorrhagic Shock

This study aims to evaluate among trauma patients with hemorrhagic shock the clinical impact of hemostatic resuscitation between whole blood vs. blood components therapy in the following outcomes in a hierarchical analysis: mortality at 28 days and evolution of organ dysfunction.

Participants needed: 220
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Fundacion Clinica Valle del LiliUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

Adult patients (> 18 years) [+3]

More than 4 hours from trauma to hospital admission [+14]

Status: Not yet recruiting

A Prospective Study Using SupraSDRM® in Promoting Healing and Reducing the Time to Grafting of Full-thickness Wounds

This is a prospective, randomized, controlled, multi-center clinical study comparing SupraSDRM® to standard of care wound dressing, BTM, in the treatment of full-thickness wounds deemed not immediately suitable for definitive grafting will be performed.

Participants needed: 24
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: The Metis FoundationUpdated: Feb 21, 2025
Eligibility criteria

Patient age ≥18 years and ≤85 years [+3]

Study wound may not include areas of the face, and neck and genitalia. [+11]

Status: Not yet recruiting

In'Oss™ (MBCP® Putty) Ortho

Study of the osteoconductive potential of the injectable bone substitute In'Oss™ (MBCP® Putty) in the filling of orthopaedic bone defects to collect Post-Market Clinical Follow-up (PMCF) data for the CE-marked In'Oss™ (MBCP® Putty) device in the orthopaedic trauma surgery

Participants needed: 100
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Advanced Medical Solutions Ltd.Updated: Feb 5, 2025
Eligibility criteria

Patient is male or female, 18 - 85 years old; [+5]

Patient has had an infection in the same extremity within last 24 months; [+16]

Status: Not yet recruiting

How Many Patients Suffering Major Trauma Would be Eligible for a Pre-hospital Transfusion

The aim of the study is to measure the number of patients being cared for by a medical team for major trauma who could benefit from a transfusion labile blood products and thus provide a scientific argument in favour of supplying labile blood products to pre-hospital

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hôpital NOVOUpdated: Dec 31, 2024Locations: 4
Eligibility criteria

Patients over 18 [+3]

Traumatological reason for departure not confirmed in the emergency medical serv... [+4]