Cardiovascular

19

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

Condition / disease
Location
Status: Recruiting

Cardiovascular Function and Response to Stimulation Within the First Year After Spinal Cord Injury

The study aims to explore how cardiovascular function changes in the first year after a spinal cord injury, and to see how different treatments, like spinal stimulation through the skin (transcutaneous spinal stimulation), affect blood pressure. The main questions are: How does stimulation affect blood pressure over the year? What is the level of cardiovascular activation throughout the year? The study will start during the inpatient stay at the Kessler Institute for Rehabilitation and continue after discharge as an outpatient, totaling about 20-29 sessions over the year.

Participants needed: 15
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Kessler FoundationUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Individuals with a spinal cord injury undergoing inpatient rehabilitation at the... [+5]

A ventilator is needed for breathing. [+9]

Status: Recruiting

Strategy for EArly Recognition of Cancer, COPD & Heart Failure in the Emergency Department

SEARCH-ED is a research study which is running in Emergency Department (ED) of the Queen Elizabeth University Hospital. The aim of the study is to find out if using a computer programme can help doctors diagnose heart and lung problems from chest x-rays. We want to compare how many people are diagnosed with heart or lung problems for the first time when doctors have access to the computer programme results, in comparison to when they don't.

Participants needed: 17,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NHS Greater Glasgow and ClydeUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Frontal Chest X-Ray (CXR) (AP or PA) acquired in the Queen Elizabeth University... [+10]

Patients not available to follow up, including patients i.e. whose the patient's... [+3]

Status: Recruiting

A Safety and Tolerability Trial Evaluating CTX310 in Participants With Refractory Dyslipidemias

This is a single-arm, open-label, multicenter, ascending dose Phase 1 trial that will enroll participants 18 to 75 years of age with dyslipidemias that are refractory to available treatments.

Participants needed: 90
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: CRISPR Therapeutics AGUpdated: May 22, 2026Locations: 18
Eligibility criteria

Age of ≥18 and ≤75 years at the time of signing the informed consent. [+5]

Participants with familial chylomicronemia syndrome (FCS). Some exceptions may a... [+6]

Status: Recruiting

Improving the Heart Health of Home Health Aides

The goal of this early-stage study is to support the heart health of home health aides, a workforce that provides care for adults at home but whose own health has been historically poor. To do this, the study will use Life's Essential 8 (LE8), a program developed by the American Heart Association (AHA) that promotes cardiovascular wellness through education and lifestyle changes. The program has been adapted specifically for home health aides and will be delivered by trained "peer coaches," who are fellow home health aides who will help guide participants through the program. The main questions the study aims to answer are: * Will the LE8 intervention, which provides cardiovascular health education and support with positive thinking, be used by home health aides and do they like it? * Does the LE8 intervention actually improve home health aides' cardiovascular health after the intervention's conclusion compared to baseline? Participants will be paired with a trained peer coach and take part in the 10-week program over the course of 6 months. The program includes support for healthy behaviors and positive thinking, with the goal of making lasting improvements in cardiovascular health.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Weill Medical College of Cornell UniversityUpdated: May 22, 2026Locations: 2
Eligibility criteria

Currently working as a home health aide [+3]

Less than 1 year of job experience as a home health aide [+3]

Status: Recruiting

Whole-life Investigation of Lishui Longevity

1. To establish a standardized, normalized and scientific joint screening and follow-up management system for chronic disease multimorbidity in Lishui City, and early identify common risk factors of major chronic diseases such as cardiovascular and cerebrovascular diseases and tumors. 2. To carry out targeted intervention and long-term follow-up for high-risk populations, reduce the incidence risk of major chronic diseases in the target population, improve residents' health status and grassroots comprehensive prevention and treatment capacity of chronic diseases, and provide scientific evidence and practical support for the construction of Healthy Lishui.

Participants needed: 4,500
Trial details
Age: 30-80Biological sex: AllType: ObservationalSponsor: The Fifth Affiliated Hospital of Wenzhou Medical University & Lishui Central HospitalUpdated: May 18, 2026Locations: 1Duration: 10 Years
Eligibility criteria

Aged 30 to 80 years old; male-to-female ratio of 1:1; permanent residents in Lis...

Individuals ever diagnosed with malignant tumors or cardiovascular and cerebrova...

Status: Recruiting

Focusing on the Menopausal Transition to Improve Mid-Life Women's Health

What if midlife women, who are inherently at an increased risk for future cardiometabolic disease due to transitioning into menopause, had access to a suite of evidence-based health interventions? Could these interventions reduce menopause-related inflammation, restore a healthier cardiometabolic profile, reverse epigenetic aging, and reduce bothersome menopausal symptoms? The ultimate goal of this work is to attenuate future disease and enhance women's quality of life, extend healthspan and increase productivity.

Participants needed: 200
Trial details
Phase: Phase 2, Phase 3Age: 45-55Biological sex: FemaleType: InterventionalSponsor: University of Colorado, DenverUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

aged 45-55 [+4]

Lack of broadband access (activity and survey data will be collected electronica... [+6]

Status: Recruiting

Collection of Blood Samples for New Diagnostic Devices 2

To research and develop new state of the art diagnostic biomarkers on the LumiraDx Platform that are comparable to the approved gold standard reference methods and will radically enhance clinicians and patients ability to monitor health conditions and improve outcomes by delivering the results near patient at the point of care.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: LumiraDx UK LimitedUpdated: Apr 22, 2026Locations: 7
Eligibility criteria

Subject 18 years of age. [+8]

Subject <18 years of age. [+2]

Status: Recruiting

The Role of EDHFs on Blood Pressure Following a Bout of Prolonged Sitting

Canadians spend most of their day in sedentary postures (i.e., sitting, lying, reclining). While the beneficial impacts of physical activity on the heart are well-established, less is known about the consequences during time spent in sedentary postures. Currently, we know that spending time in a bout of uninterrupted sitting disrupts blood pressure regulation. However, it is unknown if there are any 'carry over' effects following uninterrupted sitting bouts (i.e., over the next 24-hours). The release of chemicals from arteries controls how stiff or relaxed they are and is important for controlling blood pressure. This is especially true for arteries directly impacted by sitting (e.g., the popliteal artery behind the knee) and that send blood to the brain (e.g., the carotid artery). We have also established that endothelial-derived hyperpolarizing factors (EDHF, chemicals that relax the artery) are important for the relaxation of the artery the popliteal artery. However, we do not know if the effects of EDHFs on this artery are decreased during or after a bout of uninterrupted sitting. A bout of prolonged sitting also causes blood pressure and fluctuations in blood pressure to increase. Importantly, we reported that fluctuations in blood pressure caused by sitting are higher in young males versus females, but average blood pressure was higher among females. These findings suggest that sitting exerts sex differences in the control of blood pressure. Importantly, these effects were only demonstrated during the 2-hour bout of sitting. As such, it is unknown whether blood pressure is negatively impacted after prolonged sitting. The proposed study will determine the impact of EDHFs on blood pressure regulation following a 2-hour bout of prolonged sitting among a group of healthy males and females. Continuous heart rate (via electrocardiogram) and blood pressure (via finger cuff), as well as blood flow from the common carotid artery (in the neck), middle cerebral artery (in the brain) and popliteal artery (behind the knee) will be measured before and after sitting (via ultrasound). The ability of the popliteal artery to relax will be assessed using ultrasound following the release of a pressure cuff. Finally, 24-hour blood pressure and heart rate will be recorded after sitting using a monitor worn for 24-hours. The role of EDHFs will be investigated by comparing 1) baseline blood flow and blood pressure responses (no sitting), 2) blood pressure responses following a 2-hour bout of sitting, and 3) the blood pressure responses following a 2-hour bout of sitting while suppressing the release of EDHFs (via fluconazole ingestion).

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Université de SherbrookeUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

Are between the ages of 18-65. [+8]

o Younger than 18 years old. Individuals younger than 18 demonstrate more variab... [+12]

Status: Recruiting

Effects of Donor-recipient Sex-matched Blood Transfusion on Patient Outcomes

Red blood cell (RBC) transfusions are selected based upon matching donor and recipient blood group: donor and recipient sex are not considered when selecting blood for transfusion. Hence, transfused patients can currently receive sex-matched and/or unmatched RBCs when transfusions are given. Sex-matched stem cell transplants, and some solid organ transplants, have shown that sex-matching donor to recipient improves patient outcomes. Recent exploratory studies have also suggested that patient outcomes could be improved by sex-matching for RBC transfusion. There is emerging evidence of underlying biologic mechanism(s) to support these observations. This study is designed as a randomized controlled trial and will explore the impact on patients who receive RBC transfusions from donors of the same sex ("sex-matched") compared with donors of the opposite sex ("sex-mismatched"). The trial will study adult patients admitted to the Intensive Care Unit who require an RBC transfusion. Patients will be assigned (through a process called randomization) to receive sex-matched RBCs or sex-mismatched RBCs to determine if there is a difference in mortality between those receiving matched versus mismatched RBCs. The results of this trial could have direct implications on resources, blood inventory, and RBC transfusion ordering practices.

Participants needed: 11,082
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Michelle ZellerUpdated: Mar 12, 2026Locations: 8
Eligibility criteria

Adults (age ≥18); [+2]

Requirement for a specialized RBC product or unit not readily available in inven... [+3]

Status: Recruiting

AI Platform for Fatigue and Depression Detection

This observational study evaluates the accuracy of the Okaya AI platform in detecting fatigue and depression in cardiology patients, comparing its assessments to PHQ-9 and Fatigue Assessment Scale scores.

Participants needed: 100
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: Brijesh PatelUpdated: Feb 25, 2026Locations: 2
Eligibility criteria

Age ≥18, English-speaking, able to consent

Active substance use, nonverbal, cognitive disability, active suicidal/homicidal...

Status: Recruiting

Decoupling Immunotherapy Toxicity and Cancer Response

This study is a novel evaluation of cardiotoxicity after ICI therapy based on traditional CV risk factors with the addition of metabolomic profiles, epigenetic aging, and CHIP. It is not an extension of previous work in ICI therapy.

Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: M.D. Anderson Cancer CenterUpdated: Feb 3, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+1]

No baseline blood collection prior to initiation [+1]

Status: Recruiting

Adequate Hydration and Health Outcomes

Cardiovascular diseases (CVD) are the leading cause of death in middle- and high-income countries, according to data from the World Health Organization (WHO). Epidemiological studies have associated low water intake and underhydration with diabetes, chronic kidney disease, and an increased risk of CVD. Similarly, the prevalence of chronic metabolic dysfunction is increasing dramatically worldwide, becoming both a significant public health concern and a global economic burden. Reports from the WHO indicate that the number of people with diabetes worldwide has risen from 108 million in 1980 to 422 million in 2014, representing 8.5% of adults. Therefore, there is an urgent need to identify modifiable risk factors that could help prevent metabolic dysfunction and mitigate the epidemic of type 2 diabetes (T2D). Evidence suggests that the hormone arginine vasopressin (AVP) may play a key role. AVP is the primary hormone responsible for regulating body fluid balance; however, increased AVP secretion, such as under conditions of low water intake, appears to be a risk factor for developing diabetes. Increasing water intake may represent a simple and cost-effective way to improve glucose regulation and cardiovascular health. However, many individuals do not prefer drinking plain water, and although beverages with high sugar content may promote greater fluid intake, they also contribute additional calories that can negatively impact body weight and overall health. Thus, the central research question of this study is whether improving hydration with non-sugar-sweetened beverages can provide equivalent benefits for hydration and health outcomes in adults. Aim 1: To explore the association between habitual fluid intake and fluid preferences (water and non-sugar-sweetened beverages), hydration biomarkers, and health outcomes in normal-weight and obese adults. Aim 2: To compare the impact of increased total water intake, provided as plain water or non-sugar-sweetened beverages, on hydration, cardiovascular health, and glucose regulation in normal-weight and obese adults.

Participants needed: 144
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Arizona State UniversityUpdated: Jan 27, 2026Locations: 2
Eligibility criteria

BMI 18.5-24.9 or 30.0-39.9 kg/m2 [+3]

Diabetes [+26]

Status: Not yet recruiting

Investigation of Autonomic Stress Response Patterns in College Students With Varying Physical Activity Levels

This study aims to investigate the differences in cardiovascular stress response patterns among individuals with various physical activity levels (sedentary controls and different types of athletes). By synchronously monitoring ECG, heart rate, skin sympathetic nerve activity (SKNA), blood pressure, and cardiac output, the study will characterize physiological dynamics during resting, orthostatic challenge, cold pressor stress, and maximal exercise.

Participants needed: 60
Trial details
Age: 18-30Biological sex: AllType: ObservationalSponsor: Beijing Sport UniversityUpdated: Jan 22, 2026
Eligibility criteria

Not listed

Status: Recruiting

"Breathlessness Diagnostics in a Box" (BiaB) for Primary Care. A Multi-country Quality Improvement Project Using a Randomized Stepped-wedge Design

This prospective stepped-wedge study evaluates whether use of the Breathlessness diagnostics in a Box (BiaB) tool shortens the time to diagnosis in patients presenting with breathlessness, compared with usual care. The study is conducted in general practice settings in the Netherlands, Spain, and Portugal. Participating sites start with a usual care period and transition sequentially to the BiaB intervention period. Data are collected during routine clinical visits, from electronic medical records, and through questionnaires completed by patients and healthcare professionals.

Participants needed: 900
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: General Practitioners Research InstituteUpdated: Jan 7, 2026Locations: 3
Eligibility criteria

Patient must be at least 18 years old at the time of signing the informed consen... [+3]

Status: Not yet recruiting

Cardiometabolic and Hormonal Adaptations to 4-Month Zumba Training in Overweight/Obese Women

This study aims to evaluate the effects of a 4 month Zumba training program on cardiometabolic, hormonal, inflammatory, hepatic, renal, and functional parameters in overweight and obese women. Participants will be classified according to menopausal status (pre- or post-menopausal) and randomly assigned to an exercise group or a non-exercise control group.

Participants needed: 73
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: High Institute of Sports and Physical Education of KefUpdated: Dec 4, 2025
Eligibility criteria

Female, aged 18-65 years [+3]

Hormonal therapy or weight-loss medications [+2]

Status: Not yet recruiting

Bempedoic Acid Versus Statins in Primary-Prevention Patients With Suboptimal Statin Adherence: Effects on LDL-C Reduction and Tolerability

Bempedoic acid is an oral, non-statin LDL-cholesterol (LDL-C) lowering agent that inhibits ATP citrate lyase (ACL), upstream of HMG-CoA reductase (the enzyme inhibited by statins). MDPI +1 In patients with hypercholesterolemia who are unable to tolerate statins, or have sub-optimal statin adherence/tolerance, bempedoic acid has been shown to reduce LDL-C by \~20-30% (monotherapy) and more when added to other therapies (e.g., ezetimibe) (≈30-40%). PubMed * 2 medicinejournal.in * 2 In the large primary-prevention subgroup of the trial CLEAR Outcomes (statin-intolerant patients without prior cardiovascular event), bempedoic acid (180 mg daily) lowered LDL-C by \~21.3% and hs-CRP by \~21.5%. It also was associated with a significant reduction in major adverse cardiovascular events (MACE): hazard ratio 0.70 (95% CI 0.55-0.89) versus placebo over \~40 months. PubMed +1 Regarding tolerability: muscle-related adverse events appear lower compared to statins (because bempedoic acid is activated only in the liver, not in skeletal muscle) and it appears generally well tolerated, but there are signals of increased uric acid/gout, elevated hepatic enzymes, and creatinine/renal effects. MDPI +1 Comparative cardiovascular benefit (when normalized per unit LDL-C reduction) suggests that bempedoic acid may yield similar relative risk reductions as statins, though absolute LDL-C lowering is less.

Participants needed: 690
Trial details
Phase: Phase 3Age: 40+Biological sex: AllType: InterventionalSponsor: Sohaib AshrafUpdated: Nov 20, 2025
Eligibility criteria

Adults aged ≥40 years with no established ASCVD (no prior myocardial infarction,... [+4]

Established ASCVD (secondary prevention). [+5]

Status: Recruiting

Exercise to Slow Cardiovascular Ageing Progression

In ageing, deleterious alterations in cardiovascular (CV) structure and function increase risks of ageing-related cardiovascular disease (CVD). Investigators found that these CV alterations were associated with circulating serum metabolites, suggesting a metabolic basis to CV ageing. Investigators hypothesize that modification of these metabolites by intervention, such as exercise, may retard CV alterations and reduce CVD in ageing.

Participants needed: 450
Trial details
Age: 21-100Biological sex: AllType: ObservationalSponsor: National Heart Centre SingaporeUpdated: Jun 5, 2025Locations: 1
Eligibility criteria

Age >=21 years old [+1]

Wheelchair or bed-bound [+10]

Status: Recruiting

Virtual Ward-Assisted Very earLy dIschArge of Low-rIsk STEMI patieNTs: the VALIANT-STEMI Trial

Observational studies have suggested that early discharge (24hrs with follow up virtually by telephone) of patients who are low risk and have had successful treatment following ST elevation myocardial infarction is safe. This has not been tested in a randomised controlled trial. In this trial the study team propose to identify low risk patients and randomise them to usual care or early discharge and follow up virtually by telephone. The primary endpoint would be readmission to hospital or all cause death up to 30 day following the event. If the outcome is positive, the study will assist early discharge of patients, reduce length of stay, potentially improve patient well being and have positive financial implications for the health service

Participants needed: 600
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: The Leeds Teaching Hospitals NHS TrustUpdated: Dec 12, 2024Locations: 1
Eligibility criteria

Successful revascularisation following STEMI [+2]

Haemodynamic instability (Killip class >I) [+9]

Status: Recruiting

A Preventive, Multidisciplinary Primary Care Intervention Organized Around a Therapeutic Garden: Acceptability to Patients Suffering from Cardio-neurovascular Pathology and to Those Involved in the Action.

A preventive, multidisciplinary primary care intervention organized around a therapeutic garden: Acceptability to patients suffering from cardio-neurovascular pathology and to those involved in the action.

Participants needed: 157
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique Hopitaux De MarseilleUpdated: Oct 17, 2024Locations: 1
Eligibility criteria

age > 18 years old; [+3]

heart failure based on CNAM medical criteria (ALD n°5) stage III and IV accordin... [+5]