Echocardiography

19

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

Condition / disease
Location
Status: Recruiting

Assessment of Cardiac and Carotid Ultrasound Measurements in a Cohort of Healthy Children in Italy

This observational ambispective cohort study aims to establish reference values for cardiac structure and function, coronary artery dimensions, and carotid intima-media thickness (cIMT) in a healthy pediatric population living in Italy. Healthy children aged 0-18 years undergoing cardiologic evaluation will be enrolled. Echocardiographic and carotid ultrasound parameters will be collected together with anthropometric and demographic data. The study includes both retrospective and prospective cohorts.

Participants needed: 1,400
Trial details
Age: 0-18Biological sex: AllType: ObservationalSponsor: IRCCS Azienda Ospedaliero-Universitaria di BolognaUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

DigitHeart Echo Study

Eligible patients will be interviewed by research staff to explain the trial design and rationale. Written informed consent will be obtained from patients who voluntarily agree to participate. Demographics and medical history will be obtained. A 12-lead ECG will be performed; it has not been performed within 6 months. A photo of the 12-lead ECG will be taken by research staff using the DigitHeart-2 smartphone application. Predictions from DigitHeart-2/MERL-ECHO and other machine learning models hosted by the investigator team for each of the target anatomical and mechanical properties will be recorded. The cardiologist in charge of the patient, who is blinded to the prediction results from DigitHeart-2/MERL-ECHO, will perform echocardiography according to American Society of Echocardiography guidelines, which will serve as the gold standard for accuracy evaluation.

Participants needed: 478
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: The University of Hong KongUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

aged ≥ 18 years old [+2]

had echocardiography performed within 1 month [+4]

Status: Recruiting

COronoary Microcirculation Analysis NETwork

COMA.NET (Coronary Microcirculation Analysis Network) is a prospective, randomized, open-label, parallel-group clinical trial designed to determine whether endotype-guided pharmacotherapy is superior to standard care in improving quality of life in patients with ischemia with non-obstructive coronary arteries. Approximately 180-190 participants with objective ischemia will be randomized to either the control or the intervention group. Pharmacotherapy based on the endotype established during intracoronary assessment will be introduced in the intervention arm of the study. The primary endpoint is the change in the Seattle Angina Questionnaire (SAQ) score from baseline to 3 months. Secondary endpoints include the diagnostic accuracy of transthoracic echocardiographic coronary flow velocity reserve (CFVR), the incidence of adverse events, associations between biomarkers and coronary microvascular dysfunction (CMD), and the identification of risk factors for specific CMD endotypes. Participants will undergo invasive functional evaluation of the coronary microcirculation, measurement of echocardiographic CFVR, and analysis of selected circulating biomarkers. The study cohort will be followed up at three and six months and will include reassessment of quality of life (Seattle Angina Questionnaire, EuroQol 5-Dimensions 5-Level questionnaire, 12-item Short Form Health Survey), anxiety (Generalized Anxiety Disorder-7 score), and functional status (6-minute walk test). The study began in October 2025. Primary completion is anticipated in October 2027, and the overall study completion date is expected in March 2028.

Participants needed: 180
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Medical University of BialystokUpdated: Apr 8, 2026Locations: 1
Eligibility criteria

Angiographically significant coronary artery stenosis or FFR < 0.8 [+18]

Status: Recruiting

GLS in Difficult CPB Weaning

The goal of this observational study is to learn whether global longitudinal strain (GLS), measured by echocardiography, can predict difficulty separating from cardiopulmonary bypass (CPB) in adults undergoing elective cardiac surgery. The main questions it aims to answer are: * Can preoperative GLS measurement predict difficult separation from CPB? * Are GLS values associated with outcomes such as intensive care unit (ICU) stay, hospital stay, cardiac biomarkers, or 30-day mortality? Participants will: * Undergo standard cardiac surgery requiring CPB * Have echocardiographic assessments (TTE before and after surgery) * Have their recovery and outcomes monitored, including ICU and hospital stay, postoperative labs, and survival within 30 days

Participants needed: 213
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kartal Kosuyolu Yuksek Ihtisas Education and Research HospitalUpdated: Feb 5, 2026Locations: 2
Eligibility criteria

Age > 18 years. [+8]

Emergency cardiac surgery. [+6]

Status: Not yet recruiting

Value of Speckle Tracking Echocardiography Inflammatory Bowel Disease Patients

Value of speckle tracking echocardiography in early assessment of cardiac function in inflammatory bowel disease .

Participants needed: 100
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Assiut UniversityUpdated: Oct 2, 2025
Eligibility criteria

Age (18-60) yrs. [+2]

Patients with ischemic heart disease. -Patients with other comorbidities affecti... [+2]

Status: Recruiting

Clinical Performance Evaluation of a Diagnostic Ultrasound System

Subjects who are required to undergo transesophageal echocardiography according to the current clinical practice standards will be eligible for enrollment. Subjects will be screened for enrollment in this study against the inclusion and exclusion criteria. After successful screening and enrollment of subjects, the investigators will first use the investigational device to conduct transthoracic echocardiography (TTE), followed by transesophageal echocardiography (TEE). TEE will be conducted after the subject has been anesthetized. To avoid any delay in diagnosis and treatment, after the scan with the investigational device is completed, the probe will be reserved and the console will be switched to the existing commercial cardiac diagnostic ultrasound device in the study site for intraoperative guidance. In the study, each investigator will evaluate the overall image quality, user interface, workflow, user preferences, product preset, and functions of the system, as well as the device's safety and stability and fill out a user feedback questionnaire provided by the Sponsor.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: GE HealthcareUpdated: Sep 19, 2025Locations: 1Duration: 1 Day
Eligibility criteria

Adults ≥ 18 years old, have autonomous capacity; [+2]

Subjects who have been previously enrolled in this study or are participating in... [+4]

Status: Recruiting

A Multi-center Study on Artificial Intelligence-Based Quantitative Evaluation of Echocardiography

This project aims to collaborate with multiple medical institutions to verify the accuracy, stability, and clinical application value of AI algorithms in echocardiographic quantitative measurement through multi-center clinical research. Specific objectives include: 1. Compare the automatic measurement results of AI with the manual measurement data from physicians of different levels, and analyze the measurement deviation and consistency of AI in key parameters such as intracardiac diameter, volume, and function. 2. Investigate whether AI-assisted measurement can significantly reduce echocardiogram analysis time and optimize clinical workflows. Through multi-center data validation, establish a standardized reference system for AI ultrasound measurement, promote the promotion and application of AI technology in medical institutions at all levels, and reduce diagnostic differences between different hospitals and physicians. 3. Exploring the application of AI in special cases: Assessing the measurement stability of AI algorithms in complex cases (such as cardiomyopathy, valvular disease, coronary heart disease, etc.), and optimizing AI models to meet broader clinical needs.

Participants needed: 1,600
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: First Hospital of China Medical UniversityUpdated: Aug 21, 2025Locations: 37
Eligibility criteria

Age ≥18 - 80 years; [+8]

Patients with congenital heart disease [+1]

Status: Recruiting

Echocardiography Guided TAVR (Echo TAVR)

Conventional transcatheter aortic valve replacement (TAVR) relies on fluoroscopic and contrast agents. However, in high-risk patients, exposure to ionizing radiation and contrast agents is contraindicated and undesirable. Echocardiography guidance TAVR can offer a feasible and safer strategy for TAVR.

Participants needed: 20
Trial details
Biological sex: AllType: ObservationalSponsor: Pan XiangbinUpdated: Jun 19, 2025Locations: 1Duration: 1 Month
Eligibility criteria

symptomatic severe AS determined by echocardiography and Doppler that requiring... [+2]

Status: Recruiting

Impact of Echocardiography on Management of Critically Ill Neonates

The goal of the study was to estimate the outcome (mortality and morbidity) among hemodynamically unstable neonates, as well as the time to return to hemodynamic stability following the use of ECHO in the management of hemodynamically unstable neonates.

Participants needed: 50
Trial details
Age: 2-28Biological sex: AllType: ObservationalSponsor: Sahar Abozkaly MahmoudUpdated: Jun 3, 2025Locations: 1
Eligibility criteria

All neonates ( age 0 to 28 days) admitted to the NICU of Sohag University Hospit...

Failure to obtain informed consent . [+1]

Status: Recruiting

Integrated Echocardiography and Chest Ultrasound Assessment of Lung Recruitment in Preterm Infants

The primary aim of this work is to evaluate the role of high frequency oscillatory ventilation (HFOV) in recruitment of lung in preterm newborns 32 to 37 weeks gestational age with moderate to severe respiratory distress. The secondary aim is to evaluate the role of chest ultrasound in monitoring of lung recruitment in comparison to routine chest x ray in those babies. Also cardiac hemodynamics will be assesed using functional echocardiography.

Participants needed: 72
Trial details
Age: 1-3Biological sex: AllType: InterventionalSponsor: Alexandria UniversityUpdated: May 28, 2025Locations: 2
Eligibility criteria

Infants will be enrolled if they are 32 to 37 weeks of gestational age, have res...

Known major congenital anomalies including congenital heart diseases. [+2]

Status: Not yet recruiting

Effect of Thoracic Epidural Anesthesia on Left Ventricular Functions: A Strain Echocardiography Study

Post-thoracic surgery pain management thoracic epidural catheter is the most commonly used method. Thoracic epidural anesthesia, in which cardiac sympathetic nerves (T1-T5) are involved in neural blockade, is the focus of our research. Many studies have shown a decrease in inotropic status (intrinsic function) after blockade of cardiac sympathetic innervation with thoracic epidural anesthesia (TEA).We want to examine the cardiac effects of TEA with strain echocardiography, which is an advanced echocardiography method. Therefore, we aimed to investigate the effect of TEA on left ventricular functions with strain echocardiography.

Participants needed: 23
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Aydin Adnan Menderes UniversityUpdated: Jan 13, 2025Duration: 1 Day
Eligibility criteria

Refusal at enrollment [+8]

Status: Not yet recruiting

Effect of Left Erector Spinae Plane Block on Left Ventricular Functions

Many studies have shown a decrease in inotropic status (intrinsic function) after blockade of cardiac sympathetic innervation with thoracic epidural anesthesia (TEA) (4,5). There is no study in the literature investigating the cardiac effects of left thoracic ESP block. We think that left thoracic ESP block, like TEA, may also have cardiac effects. Therefore, we aimed to investigate the effect of left thoracic ESP block on left ventricular functions with transthoracic echocardiography (TTE).

Participants needed: 23
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Aydin Adnan Menderes UniversityUpdated: Jan 13, 2025
Eligibility criteria

Refusal at enrollment [+8]

Status: Not yet recruiting

Echo Acquisition Despite Geographic Separation by Replication of Human Movements (EAGER)

Echocardiography is a cornerstone of modern cardiology management, but access in rural and remote areas is limited. We have developed a robot ("Edler" named after the originator of echocardiography) which enables a sonographer to complete an examination at a distance. This study seeks to compare the images obtained by both methods, the completeness of the exam over a feasible time, and to identify particular components of the exam that are difficult to obtain using the robot.

Participants needed: 50
Trial details
Biological sex: AllType: InterventionalSponsor: Baker Heart and Diabetes InstituteUpdated: Dec 19, 2024Locations: 1
Eligibility criteria

Having a conventional echocardiogram

Declined consent to undergo both examinations

Status: Not yet recruiting

Effect of Small Interfering RNA Inclisiran on Carotid Plaques As Assessed by Carotid Ultrasound

Current understanding suggests that the majority of cardiovascular events are driven by vulnerable plaques. Nonetheless, the impact of PCSK9 inhibitors on the stability of carotid plaques remains insufficiently elucidated, with a notable scarcity of relevant clinical studies. This investigation seeks to address this gap through a real-world study conducted among patients with arterial sclerosis in Asia. The primary aim is to evaluate the effects of small interfering RNA (inclisiran) on carotid plaque characteristics as assessed by ultrasound, thereby contributing valuable data to inform clinical practice.

Participants needed: 40
Trial details
Phase: Phase 4Age: 18-75Biological sex: AllType: InterventionalSponsor: First Affiliated Hospital of Xinjiang Medical UniversityUpdated: Sep 19, 2024
Eligibility criteria

Patients with carotid plaques as indicated by ultrasound [+2]

- Known allergies or contraindications to PCSK9 inhibitors and/or statin therapy... [+10]

Status: Recruiting

Multimodal Cardiac Imaging Registry in Patients with Atrial Fibrillation

The goal of this observational registry is to collect a curated dataset of multimodal imaging data that will serve for development of artificial-intelligence based solutions for prediction of risk and outcomes in patients with atrial fribrillation. Type of study: observational study Study Participants: Patients with atrial fibrillation or atrial flutter who undergo clinically indicated transesophageal echocardiography before catheter ablation or cardioversion. We hypothesize, that automatic analysis of video images of transthoracic echocardiography with deep learning combined with clinical data can predict the presence of left atrial appendage thrombus (LAT). Therefore, our main aim is to create and validate an artificial intelligence model to predict the presence of LAT based on automatic analysis of transthoracic echocardiography with artificial intelligence.

Participants needed: 3,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University in Zielona GóraUpdated: Sep 4, 2024Locations: 7Duration: 12 Months
Eligibility criteria

Not listed

Status: Not yet recruiting

Beta-Blockers in Takotsubo Syndrome Study

The Beta-blockers in Takotsubo syndrome (TTS) (β-Tako) trial, is an academic, pragmatic, prospective, multicenter randomized clinical trial, aiming to assess the efficacy of beta-blockers (BB) in TTS patients. Two-hundred patients with TTS will be randomized (1:1) to BB (n=100) or no BB (n=100). BB with alpha or nitric oxide release activity will be used in the treatment arm. The primary endpoint will be the comparison of the wall motion score index by echocardiography at 7 days. A composite clinical endpoint (death, stroke, admission for recurrent TTS, ACS, heart failure or atrial fibrillation) at 1 year, will be assessed by an independent clinical events committee. Several sub-studies will be performed. The β-Tako trial will inform treatment decisions in this uniquely challenging clinical entity.

Participants needed: 200
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Spanish Society of CardiologyUpdated: Aug 26, 2024Locations: 1
Eligibility criteria

Written informed consent. [+1]

Patients diagnosed of TTS > 48 hours before. [+8]

Status: Recruiting

Normal Reference Range for Neonatal Echocardiography

Echocardiography is the main method of bedside examination of neonatal cardiac morphology, which can timely diagnose congenital heart disease and quantitatively assess its severity, but the diagnosis and evaluation process depends on the normal range of neonatal echocardiography.At present, there have been normal reference standards for echocardiography in children and adults at home and abroad, but there is no uniform standard for echocardiographic parameters in newborns, especially premature infants.This study intends to carry out a national multicenter, prospective, observational study to establish the reference range of echocardiography at different time periods after birth in newborns, and stratified according to gestational age, birth weight and gender, to conduct a more accurate hemodynamic assessment of clinically critically ill newborns and guide the treatment of critically ill newborns in real time.

Participants needed: 1,500
Trial details
Age: 1-28Biological sex: AllType: ObservationalSponsor: Children's Hospital of Chongqing Medical UniversityUpdated: Jul 16, 2024Locations: 1
Eligibility criteria

Outpatient or inpatient neonate [+5]

specialist cardiac ultrasound suggests congenital heart disease; [+10]

Status: Recruiting

Algorithms to Improve the Accuracy of the Echocardiographic Report

This observational study aims to improve the accuracy of the report of the echocardiographic study, making it more consistent with the current international guidelines and reducing the diagnostic mistakes in patients undergoing clinically -indicated echocardiography. The main questions it aims to answer are: * can the addition of automated diagnostic algorithms help to improve the overall accuracy of the echocardiographic report?

Participants needed: 3,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istituto Auxologico ItalianoUpdated: Apr 16, 2024Locations: 1
Eligibility criteria

Having undergone a clinically-indicated echocardiographic study

Denial of the consensus to use individual clinical data for research purposes

Status: Not yet recruiting

Preoperative Focused Cardiac Ultrasound in Hip Fracture Surgery (PrEcho)

The primary objective of this study is to investigate the impact of preoperative focused transthoracic ultrasound (FOCUS) on intraoperative hypotension and postoperative complications in hip fracture surgery. Our hypothesis is that a preoperative FOCUS along with a hemodynamic optimization protocol will reduce the occurrence of intraoperative drops in blood pressure and post-operative complications.

Participants needed: 100
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Umeå UniversityUpdated: Dec 8, 2023
Eligibility criteria

Patients ≥ 65 years of age, with American Socieity of Anesthesiologists (ASA) ph...

Metastatic cancer and/or suspect pathological fracture. [+4]