Clinical trials

146

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Metformin and ACLR Muscle Recovery

The purpose of this research study is to determine if Metformin taken after anterior cruciate ligament reconstruction (ACLR) surgery can decrease muscle fibrosis, cellular senescence and improve leg strength. ACL injury and surgery increase muscle collagen content and inflammation which slows the recovery of muscle and function and ultimately impacts the quality of life. Individuals enrolled in the study will be randomized to receive metformin (or placebo) for 4 months after surgery. The investigators will measure muscle strength and inflammatory markers in muscle biopsy samples after the intervention period. Investigators will also follow up with participants 8 months later to determine the lasting effects of the intervention.

Participants needed: 40
Trial details
Phase: Early Phase 1Age: 40+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Age between 40y and older [+3]

Prior ACL tear in limb scheduled for reconstruction or current bilateral ACL tea... [+18]

Status: Not yet recruiting

AI-Driven Survivorship Care Plans (AI-SCP)

This project conducts exploratory work on a HIPAA-compliant, large language model (LLM)-based tool that integrates structured and unstructured oncology electronic health record (EHR) data to automate the development of tailored SCPs, paired with a patient-facing chatbot to answer questions about the SCP. Unlike generic AI documentation tools, this system establishes benchmarks for SCP development and embeds user-centered design (UCD) directly into prompt engineering and model governance workflows.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Adult cancer survivors [+3]

Under age 18 [+2]

Status: Not yet recruiting

Digital Technology-Informed Stroke Rehabilitation

The goal of this study is to determine the effects of lab and home-based technology guidance during movement training post-stroke. The study will compare movement training informed by lab-based technology to training delivered with technology at home. The main questions it aims to answer are: * How well do lab and home-based technologies help individuals post-stroke improve their movement patterns? * Is there a difference in improvement between the in-lab and at-home training groups? * Which technologies lead to the most improvement?

Participants needed: 60
Trial details
Age: 30-85Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Age between 30-85 years. [+5]

Presence of severe aphasia preventing the ability to follow 1-step directions at... [+7]

Status: Recruiting

Neoadjuvant Ipilimumab/Nivolumab for Patients With Recurrent, High Risk, Resectable Melanoma

The goal of this clinical trial is to study the impact of Neoadjuvant ipilimumab and nivolumab for melanoma patients that had recurrence during or after adjuvant anti-PD-1 therapy. Participants will receive 2 cycles of treatment prior to their standard of care surgery. After surgery participants will receive standard of care adjuvant therapy and be followed for response.

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Subjects aged ≥ 18 years. [+17]

Prior exposure to anti-CTLA4 therapy. [+20]

Status: Recruiting

Pilot Study of Anti-CD19 Chimeric Antigen Receptor T Cells (CAR-T Cells) for the Treatment of Relapsed/Refractory CD19+ Malignancies

This is an open label, non-randomized, phase 1 study of anti-CD19 CAR-T cells against relapsed CD19 positive NHL, CLL and ALL based in a lymphodepletion regimen (fludarabine and cyclophosphamide) and using a CellReGen-based process for manufacturing CAR-T cells. This study will utilize a staggered enrollment design with a safety observation period.

Participants needed: 10
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Subjects aged ≥ 18 years. [+30]

Autologous or allogeneic stem cell transplant or CAR-T therapy within 6 weeks of... [+20]

Status: Recruiting

Stereotactic Radiosurgery Dose Escalation for Brain Metastases

This is a Phase I dose escalation and expansion trial. The purpose of this study is to determine the maximum tolerated dose of radiation received during stereotactic radiosurgery in patients with brain metastases who have never received radiation to the brain before.

Participants needed: 86
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Clinically confirmed brain metastases by CT or MRI criteria. If there is evidenc... [+14]

Prior whole brain irradiation. [+7]

Status: Recruiting

Culturally Engaged REcovery: MOms Connected Through Native communitY

Pregnant and postpartum American Indian and Alaska Native people (Native mothers) face a more than two-fold higher risk of maternal mortality compared to non-Hispanic White mothers. Deaths related to substance use (SU) and mental health conditions are a leading cause of preventable maternal mortality, including among Native mothers, making these conditions a strong target for reducing maternal mortality and morbidity. The objective of this study is to 1) adapt evidence-based perinatal care models that integrate pregnancy and postpartum care with SU treatment and care to meet the needs of Native mothers, and 2) assess the implementation and efficacy of that model for participants with substance use disorder who identify as Native receiving prenatal care at Sacred Circle Healthcare in Salt Lake City, Utah.

Participants needed: 270
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: University of UtahUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

English or Spanish speaking [+4]

have a documented psychotic episode in the last 30 days [+4]

Status: Recruiting

Financial Counseling for Dementia Family Caregivers in Early and Middle Adulthood

The goal of this National Institutes of Health (NIH) Stage 1a study is to develop and pilot test a research- and community-informed financial counseling and advocacy (FCA) intervention for dementia family caregivers in early and middle adulthood. The main question it aims to answer is: Is a research- and community-informed financial counseling and advocacy intervention usable, feasible and acceptable for dementia family caregivers in early and middle adulthood? Participants will engage in a four-week single group financial counseling and advocacy intervention and complete pre- and post-intervention measures addressing financial well-being, caregiver strain, workplace productivity, and flourishing along with usability, acceptability, and feasibility measures.

Participants needed: 10
Trial details
Age: 25-55Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Caring for a family member, neighbor, or friend with ADRD [+3]

N/A

Status: Recruiting

XL092 in Patients With Metastatic Castration-Resistant Prostate Cancer

The purpose of this study is to determine how well the study drug XL092 is helping to treat a participant's cancer after 16 weeks of treatment. Researchers will also look at how safe the XL092 is and how well the XL092 is working. XL092 is an oral tablet that will be taken once a day. Participants will return to clinic for regular visits for checkups and tests.

Participants needed: 32
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: University of UtahUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Participant aged ≥ 18 years [+13]

Prior treatment with XL092 [+41]

Status: Recruiting

Loncastuximab Tesirine and Rituximab Following Stereotactic Radiosurgery in Patients With Central Nervous System Lymphomas (SOLAR)

The purpose of this clinical trial is to learn if drugs loncastuximab tesirine and rituximab (lonca-R) after stereotactic radiosurgery are safe and effective for treatment of central nervous system lymphomas.

Participants needed: 12
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 29, 2026Locations: 3
Eligibility criteria

Participant aged ≥ 18 years [+20]

Concurrent use of other approved or investigational antineoplastic agents (with... [+19]

Status: Not yet recruiting

FOCUS Pre-Post Study

The Facilitating Goal-based Conversations for Understanding Surgery (FOCUS) Guide is a communication intervention designed to support discussion and documentation of the goal for surgery during outpatient surgical consultations. The purpose of this study is to assess the efficacy of the FOCUS guide in prompting discussion of the goal for surgery.

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 26, 2026
Eligibility criteria

Age ≥65 years. [+3]

Surgeons with a predominantly pediatric practice [+6]

Status: Not yet recruiting

Brief Postoperative Pain Management Intervention: Meaning Making Amendment

This single-site, two-arm, parallel-group randomized controlled trial will enroll adults undergoing total knee or hip replacement surgery. Two days after surgery, participants will complete a brief guided mindful breathing practice delivered by text message and will then be randomized to receive either personalized meaning-making questions or implementation-focused questions. The trial will evaluate whether personalized meaning-making questions enhance the clinical effects of the mindfulness practice on acute pain, pain unpleasantness, anxiety, desire for pain medication.

Participants needed: 576
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Age ≥18, [+1]

Inability to read English [+1]

Status: Recruiting

Optimizing Cardiovascular Preventive Care for Women Following Hypertensive Disorders of Pregnancy

Cardiovascular disease is the leading cause of death among women in the United States, and women with hypertensive disorders of pregnancy have a 2-fold higher risk for cardiovascular disease later in life compared to women with uncomplicated pregnancies. This research investigates a patient-centered intervention during the postpartum period to promote engagement in cardiovascular preventive care.

Participants needed: 30
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of UtahUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Delivered a pregnancy complicated by a hypertensive disorder of pregnancy at the... [+2]

Cardiovascular disease diagnosis (history of peripheral artery disease, stroke,... [+1]

Status: Recruiting

Optimal PSA Triggered Individual Management of Androgen Sensitive Prostate Cancer

The purpose of this study is to evaluate intermittent relugolix + androgen receptor pathway inhibitor (ARPI) in patients with metastatic hormone-sensitive prostate cancer (mHSPC) achieving optimal PSA response.

Participants needed: 160
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: University of UtahUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Participant aged ≥ 18 years [+22]

Participant received androgen deprivation therapy (defined as leuprolide or surg... [+18]

Status: Recruiting

Lesion-tailored, Fundus-controlled Perimetry in Geographic Atrophy (GA).

The goal of this observational study is to evaluate changes in retinal sensitivity over time in patients with geographic atrophy due to age related macular degeneration who are receiving pegcetacoplan as part of routine clinical care. The study aims to determine whether lesion tailored fundus-controlled perimetry can reliably measure functional changes near areas of atrophy and whether this testing can be implemented in everyday clinic care over 24 months. Participants will undergo repeated vision testing, standard eye imaging, and visual function questionnaires while continuing their prescribed treatment.

Participants needed: 50
Trial details
Age: 65-90Biological sex: AllType: ObservationalSponsor: University of UtahUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Age 65-90 years. [+7]

Currently or previously active exudative macular neovascularization in the study... [+4]

Status: Recruiting

Rural Adult and Youth Sun Protection Study

The purpose of this study is to help prevent skin cancer by improving the use of sun protective behaviors among youths living in rural communities in Utah and West Virginia.

Participants needed: 843
Trial details
Age: 3-7Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 12, 2026Locations: 2
Eligibility criteria

Adults and children who do not speak or read English will be excluded. [+1]

Status: Recruiting

Microvideos for Improving HPV Vaccination Among Childhood Cancer Survivors

This exploratory mixed-methods study aims to examine receipt of treatment and decision-making among rural cancer patients in Utah. Guided by Conceptual Model of Healthcare Access, the study will integrate, survey and cancer registry data with patient interviews to better understand how travel burden, socioeconomic conditions, health literacy, and other contextual factors shape treatment location and access to care . While the setting of this research is specific to Utah, a state with vast rural regions and only one National Cancer Institute (NCI)-designated cancer center, the findings may inform policy and practice improvements in other states with similar geographic and healthcare infrastructure. Thus, the study has potential relevance for advancing rural cancer equity nationwide. Understanding how rural cancer patients make treatment decisions is essential to addressing persistent disparities in cancer care access and outcomes. While geographic barriers and structural inequities are well-documented, less is known about the individual and contextual factors that shape patients' choices about where and how to receive treatment. This mixed-methods study will examine receipt of treatment, decision-making, and patient experience among rural cancer patients in Utah, with attention to travel burden, referral pathways, health literacy, and perceived barriers to care.

Participants needed: 55
Trial details
Age: 18-26Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 15, 2026Locations: 1
Eligibility criteria

Eligible participants include cancer survivors who are currently ages 18-26 year... [+2]

Unable to speak and understand English. [+2]

Status: Recruiting

Scaling up Building Healthy Families

Evidence-based interventions for childhood obesity (EBI-CO) can improve children's weight status, but families in rural areas and small cities have limited access to the interdisciplinary healthcare teams recommended to deliver EBI-CO. To address this issue, the investigators adapted an EBI-CO, Building Healthy Families (BHF), which includes all materials and training resources necessary for rural program implementation. The pilot study found that when paired with opportunities to learn from the program developers and other community implementation teams, the packaged program led to effective delivery across 4 rural communities. This scale-up study will compare packaged BHF Resources with and without a learning collaborative facilitation strategy, examining outcomes including reach, effectiveness, implementation, and potential for sustainability in rural areas.

Participants needed: 150
Trial details
Age: 5+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Any community is eligible to apply for the competitive BHF RFA process; [+7]

Status: Not yet recruiting

SAFE.AI: Developing and Testing an AI-based Hybrid Chatbot for Financial Empowerment in Rural Cancer Care

This is a randomized, two-arm, parallel-group pilot trial investigating a new chatbot tool designed to support cancer patients and caregivers, particularly those in rural communities. Approximately 60 participants will be randomized 1:1 to interact with either a hybrid chatbot or an AI-enabled chatbot. Participants will use their assigned chatbot to obtain clear and helpful information related to insurance, travel costs, and other financial aspects of cancer care.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Adults (18 years and older) [+3]

Respondents who do not live within this 5-state region--The SAFE toolkit materia... [+3]

Status: Recruiting

Impact of Budesonide on Incidence of ≥ Gr2 Diarrhea in Multiple Myeloma (MM) Patients Undergoing Autologous Stem Cell Transplant

A randomized placebo controlled, phase 2 study of budesonide in subjects with multiple myeloma undergoing autologous stem cell transplant (ACST). The study includes a run-in period with 20 patients.

Participants needed: 120
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Subject aged ≥ 18 years. [+11]

Ongoing or current use of oral budesonide at the time of enrollment. [+7]

Status: Recruiting

Cabozantinib and Atezolizumab for the Treatment of Metastatic Castration-Resistant Prostate Cancer

This phase II trial tests whether cabozantinib and atezolizumab work to shrink tumors in patients with castrate-resistant prostate cancer that had spread to other places in the body (metastatic). Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving cabozantinib and atezolizumab may kill more tumor cells in patients with metastatic castrate-resistant prostate cancer.

Participants needed: 33
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: University of UtahUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Male subject aged >= 18 years [+25]

Prior chemotherapy in the metastatic castration refractory prostate cancer setti... [+61]

Status: Recruiting

External Beam Radiotherapy Followed by Bispecific Antibody Therapy for Relapsed/Refractory DLBCL

The purpose of this clinical trial is to assess the safety and tolerability of ration therapy followed by receiving epcoritamab or glofitamab in patients with relapsed/refractory diffuse large B-cell lymphoma.

Participants needed: 12
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Participant aged ≥ 18 years [+20]

Currently receiving any other approved or investigational therapy considered as... [+11]

Status: Recruiting

AlloHCT With PegINFa for Myelofibrosis

This is a single site, open-label, dose de-escalation, Phase 1 study of pegylated interferon alfa-2a administered after alloHCT in subjects with primary or secondary myelofibrosis. Part 1 of the study will assess the rate of dose-limiting toxicities (DLTs) during the DLT evaluation period and identify the Recommended Phase 2 Dose (RP2D). Once the RP2D is identified, 6 additional patients will be enrolled in the expansion cohort.

Participants needed: 18
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Male or female subject aged ≥ 18 years. [+34]

Receiving other investigational agents concurrently [+18]

Status: Not yet recruiting

LLM Intervention for Tobacco in Underserved Populations (LIFT-UP)

This study will test a tailored, multilingual tobacco cessation chatbot called LIFT-UP (LLM Intervention for Tobacco in Underserved Populations), designed to better meet the needs of people living in persistent poverty census tracts. This study will use 1:1 semi-structured interviews to explore social drivers of health impacting TC, as well as digital access and preferences among those living in PPCTs. This qualitative approach enables guided yet flexible exploration of key domains while capturing unanticipated insights relevant to refining the chatbot.

Participants needed: 22
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

18+ years old [+5]

None

Status: Recruiting

Creatine Supplementation and Resistance Training to Preserve Muscle Mass and Attenuate Cancer Progression

The goal of this clinical trial is to test the use of creatine monohydrate supplementation with resistance training to preserve muscle mass and help lessen prostate cancer progression. The main question it aims to answer is if this treatment will help maintain muscle mass to help in reducing fatigue and improving physical function, independence, and quality of life. Participants will be asked to participate in a 52-week exercise intervention consisting of a twice weekly telehealth resistance training program.

Participants needed: 200
Trial details
Phase: Phase 3Age: 18+Biological sex: MaleType: InterventionalSponsor: University of UtahUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

Subject age ≥ 18 years old. [+11]

Treatment with cytotoxic chemotherapy within 12 weeks prior to enrollment. [+2]