Left Ventricular Dysfunction

14

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

Condition / disease
Location
Status: Not yet recruiting

PASCAL Precision-GDMT Registry

The goal of this observational study is to demonstrate that successful tricuspid valve repair with the PASCAL Precision System in participants with at least severe tricuspid insufficiency and left ventricular dysfunction will be associated with an improvement in up-titration of guideline-directed medical therapy (GDMT). The main question it aims to answer is: Does the tricuspid insufficiency repair with the Pascal Precision System increases the dose of the medications used for heart failure therapy in the study population 12 months after tricuspid repair, as compared to the dose taken at baseline. Participants undergoing tricuspid repair and fulfilling all inclusion/exclusion criteria will be asked to answer heart failure assessment as well as quality of life questionnaires at baseline and at 12 months post intervention. Medication monitoring will be performed throughout the study.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ceric SàrlUpdated: May 13, 2026Duration: 12 Months
Eligibility criteria

Participants of age ≥ 18 years [+5]

Anatomy unsuitable for TEER as determined by local heart team [+13]

Status: Not yet recruiting

Menopausal Hormone Therapy And Left Ventricular Function

The purpose of this study is to compare left ventricular stroke volume and heart rate responses to bursts of SNA between PMF using, and not using, MHT.

Participants needed: 50
Trial details
Age: 45-60Biological sex: FemaleType: ObservationalSponsor: Mayo ClinicUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Male sex [+17]

Status: Recruiting

The JenaValve ALIGN-AR LVAD Registry

To evaluate the safety and effectiveness of the JenaValve Trilogy™ Heart Valve System for transcatheter aortic valve replacement (TAVR) in subjects with continuous flow left ventricular assist devices (cfLVAD) and clinically significant aortic regurgitation (AR) who are indicated for TAVR

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: JenaValve Technology, Inc.Updated: Apr 1, 2026Locations: 15
Eligibility criteria

Patient with NYHA functional class III/IV [+4]

Congenital uni- or bicuspid (Sievers 0) aortic valve morphology [+20]

Status: Recruiting

London Valvular Heart Disease and Reduced Ejection Fraction Detection in a Multi-ethnic Community Using Cardiac Ultrasound

Heart Valve Disease and Heart failure contribute to 25% of hospital emergency admissions while heart failure alone has become one of the most common causes for hospitalisation in people over the age of 65. The burden of disease is likely to be high in a multi-ethnic community but there is a paucity of data. Management of heart valve disease requires appropriate surveillance and timely surgery. Similarly heart failure management requires treatment with medications aimed at slowing prevention of symptoms and preventing premature death. The NHS long term plan priorities early detection and treatment of valve disease and heart failure in order to reduce the burden on emergency services and improve the health of the population. Diagnosis is made using cardiac ultrasound, however staff with the required skills-set are critically limited in the community. The investigators will train non-expert staff within primary care to perform abbreviated cardiac ultrasound to detect heart valve disease or heart failure. This will be opportunistic scanning to reduce healthcare footfall. All scans will be reviewed by an expert and the investigators will use the anonymised data to develop machine learning tools to begin working with academic partners to develop tools that can improve the reliability of diagnosis from ultrasound. The investigators hope to identify the proportion with the above conditions in a multi-ethnic community and assess the feasibility of developing a program where staff can be trained for community detection, streamlined referrals can be created bridging the gap between primary and secondary care, reducing hospital emergency admissions, while ensuring patients are managed optimally.

Participants needed: 500
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Queen Mary University of LondonUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Clinical diagnosis of Alzheimer's Disease or Vascular Dementia [+1]

Status: Recruiting

DAPAgliflozine to Attenuate Cardiac RemOdeling afTEr aCuTe myOcardial Infarction

Recent clinical trials have proven the cardiovascular benefits of new medications for patients with heart failure with reduced ejection fraction (HFrEF), especially sodium-glucose co-transporter 2 (SGLT2) inhibitors. There are no existing randomized clinical trials evaluating the efficacy and safety of dapagliflozin (nor any other SGLT2-inhibitor) to limit cardiac remodeling in patients with acute myocardial infarction (AMI) and left ventricular (LV) dysfunction. Preventing cardiac remodeling, an established predictor of subsequent heart failure (HF) and cardiovascular death, is likely to translate into benefit in reducing clinical events in post-MI patients.

Participants needed: 450
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Dec 19, 2025Locations: 1
Eligibility criteria

Age ≥18 years; [+5]

Cardiogenic shock (SBP <90 mmHg with clinical signs of low output or patients re... [+14]

Status: Recruiting

Pediatric Hypertension and the Renin-Angiotensin SystEm (PHRASE)

Studying the causal roles of components of the renin-angiotensin-aldosterone system (including angiotensin-(1-7) (Ang-(1-7)), angiotensin-converting enzyme 2 (ACE2), Ang II, and ACE), uric acid, and klotho in pediatric hypertension and related target organ injury, including in the heart, kidneys, vasculature, and brain. Recruiting children with a new hypertension diagnosis over a 2-year period from the Hypertension and Pediatric Nephrology Clinics affiliated with Brenner Children's Hospital at Atrium Health Wake Forest Baptist and Atrium Health Levine Children's Hospital. Healthy control participants will be recruited from local general primary care practices. Collecting blood and urine samples to analyze components of the renin-angiotensin-aldosterone system (Ang-(1-7), ACE2, Ang II, ACE), uric acid, and klotho, and measuring blood pressure, heart structure and function, autonomic function, vascular function, and kidney function at baseline, year 1, and year 2. Objectives are to investigate phenotypic and treatment response variability and to causally infer if Ang-(1-7), ACE2, Ang II, ACE, uric acid, and klotho contribute to target organ injury due to hypertension.

Participants needed: 125
Trial details
Age: 7-18Biological sex: AllType: ObservationalSponsor: Wake Forest University Health SciencesUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

7-18 years of age at time of enrollment [+4]

<7 years or >18 years of age at time of enrollment [+24]

Status: Not yet recruiting

Assement of Left Ventricular Function Before Decannulation in Cardiac Surgery :Visual Estimation vs TEE

This study aims to evaluate the diagnostic performance of the cardiovascular surgeon's visual estimation of LV function before decannulation following cardiopulmonary bypass, using TEE results as the reference standard.

Participants needed: 70
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Ataturk UniversityUpdated: Dec 16, 2025Locations: 1
Eligibility criteria

Age between 18 and 75 years [+4]

Emergency surgery [+5]

Status: Recruiting

Prevalence and Risk Factors asSOciated With CArdiac comorbiDIty in psoriAsis

In a prospective cohort study (n = 1.000), the investigators aim to investigate the correlation between cardiac biomarkers and advanced echocardiography and determine whether these are prognostic markers of heart disease in patients suffering from psoriasis.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Herlev and Gentofte HospitalUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Patients 18 years or older with a diagnosis of psoriasis will be invited to part...

Patients not able to cooperate to the study [+1]

Status: Recruiting

Conventional Biventricular Versus Left Bundle Branch Pacing on Outcomes in Heart Failure Patients

Heart failure (HF) is the most common nosology encountered in clinical practice. Its incidence and prevalence increase exponentially with increasing age and it is associated with increased mortality, more frequent hospitalization and decreased quality of life. An initial approach to the treatment of HF patients with reduced left ventricular (LV) systolic function and left bundle branch block (LBBB) was implantation of cardioresynchronization device using biventricular pacing. This has resulted in long-term clinical benefits such as improved quality of life, increased functional capacity, reduced HF hospitalizations and overall mortality. However, conventional cardiac resynchronization therapy (CRT) is effective in only 70% of patients. And the remaining 30% of patients are non-responders to conventional CRT. Subsequently, His bundle pacing (HBP) has been developed to achieve the same results. According to other studies HBP has showed greater improvement in hemodynamic parameters than with conventional biventricular CRT. But, nevertheless, there are significant clinical troubles with HBP. In this regard, in 2017, the left bundle branch pacing (LBBP) was developed, which demonstrated clinical advantages compared to biventricular CRT. This method has become an alternative to HBP due to the stimulation of LBB outside the blocking site, a stable pacing threshold and a narrow QRS duration. A series of case reports and observational studies have demonstrated the efficacy and safety of LBBP in patients with CRT indications. However, it is not enough data about CRT with LBBP effectiveness in LV remodeling, reducing mortality and complications. According to our hypothesis, CRT with LBBP compared with conventional biventricular CRT will significantly improve the clinical outcomes and reverse LV remodeling in patients with chronic HF with reduced LV ejection fraction and reduce the number of non-responders to conventional CRT.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Tomsk National Research Medical Center of the Russian Academy of SciencesUpdated: Sep 10, 2025Locations: 1
Eligibility criteria

The patient is willing and able to comply with the protocol and has provided wri... [+11]

Coronary artery (CA) bypass grafting, balloon dilatation or CA stenting within 3... [+20]

Status: Not yet recruiting

Preoperative Maltodextrin's Effect on Cardiac Function in Cardiac Surgery

A randomized, controlled, double-blinded clinical trial evaluating the effect of the administration of a Maltodextrin solution on cardiac function in patients presenting for coronary artery bypass grafting surgery with a reduced left ventricular ejection fraction.

Participants needed: 70
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Jewish General HospitalUpdated: Feb 24, 2025Locations: 1
Eligibility criteria

18 years of age or older [+3]

Dysphagia, gastroparesis [+3]

Status: Recruiting

Left Bundle Branch Pacing on Outcomes and Ventricular Remodeling in Biventricular CRT Nonresponders

Heart failure (HF) is the most common nosology encountered in clinical practice. Its incidence and prevalence increase exponentially with increasing age and it is associated with the increased mortality, more frequent hospitalization and decreased quality of life. An initial approach to the treatment of HF patients with reduced left ventricular (LV) systolic function and left bundle branch block (LBBB) was implantation of device for cardiac resynchronization therapy using biventricular pacing. This has resulted in long-term clinical benefits such as improved quality of life, increased functional capacity, reduced HF hospitalizations and overall mortality. However, conventional cardiac resynchronization therapy (CRT) is effective in only 70% of patients. And the remaining 30% of patients are non-responders to conventional CRT. Cardiac conduction system pacing is currently a promising technique for these patients. Particularly, His bundle pacing (HBP) has been developed to achieve the same results. According to other studies HBP has shown greater improvement in hemodynamic parameters comparing with conventional biventricular CRT. But, nevertheless, there are significant clinical troubles with HBP, especially high pacing threshold. In this regard, in 2017, the left bundle branch pacing (LBBP) was developed, which demonstrated clinical advantages compared to conventional biventricular CRT. Also, since 2019, left bundle branch pacing-optimized CRT (LBBPO CRT) has been used in clinical practice. These methods have become an alternative to HBP due to the stimulation of LBB outside the blocking site, a stable pacing threshold and a narrow QRS complex duration on electrocardiogram. A series of case reports and observational studies have demonstrated the efficacy and safety of LBBP and LBBPO CRT in patients with CRT indications. However, it is not enough data about impact of CRT with LBBP and combined CRT with LBBP and LV pacing on myocardial remodeling, reducing mortality and complications. According to our hypothesis, CRT with LBBP and combined CRT with LBBP and LV pacing compared with conventional biventricular pacing will significantly improve the clinical outcomes and reverse myocardial remodeling in patients who are non-responders to biventricular CRT with HF, reduced LV ejection fraction and with indications to CRT devices with defibrillator function (CRT-D) or one of the CRT-D leads replacement.

Participants needed: 30
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Tomsk National Research Medical Center of the Russian Academy of SciencesUpdated: Nov 22, 2024Locations: 1
Eligibility criteria

The patient is willing and able to comply with the protocol and has provided wri... [+6]

Coronary artery (CA) bypass grafting, balloon dilatation or CA stenting within 3... [+20]

Status: Recruiting

Sodium Lowering Vascular Effects Trial

The proposed mechanistic trial will test the effect of dietary sodium reduction on cardiac and vascular structure and function in those with elevated blood pressure or hypertension. Findings from this study will fill the knowledge gap on the underlying mechanisms of dietary sodium intake on cardiovascular disease risk in addition to blood pressure and could provide further evidence on sodium reduction for the prevention of cardiovascular disease.

Participants needed: 256
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Tulane UniversityUpdated: Nov 22, 2024Locations: 1
Eligibility criteria

Men or women aged ≥40 years. Individuals <40 years are at a low risk for clinica... [+1]

Glomerular filtration rate (eGFR) <30 or end-stage renal disease (kidney transpl... [+8]

Status: Recruiting

Reducing Cognitive Impairment by Management of Heart Failure as a Modifiable Risk Factor

This study will test the feasibility and effectiveness of an innovative model of care for cognitively impaired patients with heart failure. This program aims to improve cognition, reduce dementia risk and cardiovascular events, and will be supported by innovative digital technology for wide scale rollout and implementation. Findings from this research will transform the way healthcare is delivered to cognitively impaired patients with heart disease who have a very high risk of developing dementia.

Participants needed: 168
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Baker Heart and Diabetes InstituteUpdated: Aug 12, 2024Locations: 1
Eligibility criteria

Hospitalised with HF as primary or secondary diagnosis. [+1]

Unable to provide written consent; requiring palliative care; or participating i... [+2]

Status: Recruiting

Microvascular Dysfunction Assessment to Predict Left Ventricular Reverse Remodeling

Patients presenting with idiopathic dilated cardiomyopathy and left ventricle dysfunction (LVEF \<40%), naive of anti-remodeling cardiac medical therapy, will undergo invasive coronary microvascular assessment based on thermodilution. The primary endpoint, namely the left ventricle reverse remodeling, will be assessed after 12 months of optimal medical therapy based on transthoracic echocardiography. The primary endpoint will be evaluated by an independent central core lab. Patients enrolled in the study will be followed for a period of 5 years to monitor their clinical status. During the study period participants may undergo multimodality diagnostic tests including ECG telemetry monitoring, cardiopulmonary exercise testing, cardiovascular cardiac magnetic resonance.

Participants needed: 190
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Azienda Ospedaliera Universitaria Integrata VeronaUpdated: Apr 10, 2024Locations: 9
Eligibility criteria

Male or female, aged >18 years [+2]

Obstructive CAD (defined as angiographically intermediate disease [50%-70%] with... [+14]