Heart Failure, Congestive

6

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

Condition / disease
Location
Status: Recruiting

Diuretics Alone vs. Aortix Endovascular Device for Acute Heart Failure

Aortix is a circulatory support device for chronic heart failure patients on medical management who have been hospitalized for acute decompensated heart failure (ADHF) and have persistent congestion despite usual medical therapy. Eligible ADHF patients with diuretic resistance (irrespective of ejection fraction) will be enrolled and randomized 1:1 to either the Aortix system or standard of care medical management.

Participants needed: 320
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: ProcyrionUpdated: Jun 9, 2026Locations: 48
Eligibility criteria

Currently admitted to the hospital with a primary diagnosis of decompensated hea... [+4]

Treatment with high dose IV inotropes within the last 48 hours prior to enrollme... [+71]

Status: Recruiting

Magnetic Resonance Spectroscopy Studies of Cardiac Muscle Metabolism

The metabolism of the heart provides the chemical energy needed to fuel ongoing normal heart contraction. Magnetic resonance spectroscopy is a technique used in a MRI scanner that can be used to measure and study heart metabolism directly but without blood sampling or obtaining tissue biopsies. One of the hypotheses this study aims to investigate is whether energy metabolism is reduced in heart failure and whether that contributes to the poor heart function.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Johns Hopkins UniversityUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

age > 18 years [+4]

contraindication to MRI

Status: Recruiting

Prospective Observational Study of the ICD in Sudden Cardiac Death Prevention

The overall hypothesis of this study is that subtle interactions between structural (substrate) and functional (trigger) abnormalities of the heart, some of which are genetically-determined, can be used to identify patients at high risk of sudden cardiac death (SCD). Such information may be used to better define patients most likely to benefit from replacement of an internal defibrillator (ICD). The prospective, observational study to enroll, categorize and follow patients who receive an ICD pulse generator replacement for primary prevention of SCD (PROSe-ICD) was established to : 1. to gain a better understanding of the biological mechanisms that predispose to SCD 2. to develop readily determined clinical, electrocardiographic, genetic and blood protein markers identify patients with an increased risk of dying suddenly

Participants needed: 1,500
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Johns Hopkins UniversityUpdated: Jan 20, 2026Locations: 4
Eligibility criteria

History of acute MI at least 4 weeks old [+4]

ICD generator replacement for secondary prevention [+3]

Status: Recruiting

Effect of Losartan on the Neurohumoral Axis and Ventricular Remodeling of Patients With Severe Aortic Regurgitation Undergoing Valve Surgery.

Why Is This Study Important? The heart has valves that help control blood flow. Aortic regurgitation (AR) is a condition where one of these valves (the aortic valve) doesn't close properly, causing blood to leak back into the heart. Over time, this makes the heart work harder and grow larger (remodeling) to keep up. Many patients with severe AR need valve replacement surgery to fix this problem. After surgery, the heart doesn't have to work as hard, and over time, it can shrink back to a healthier size (reverse remodeling). However, doctors don't know if medications can help speed up or improve this healing process. This study aims to find out if a common blood pressure medication, losartan, can help the heart recover better after surgery. What Do the Investigators Already Know? Doctors often prescribe medications like ACE inhibitors, angiotensin receptor blockers (ARBs), beta-blockers, and spironolactone to people with heart failure because these drugs help the heart function better and prevent worsening disease. However, these medications haven't been studied in people with valve disease because most major research studies excluded patients with valve problems. Even though there is not strong evidence, many doctors prescribe these medications after valve surgery, assuming they might be helpful. But is that really the case? That's the question this study hopes to answer. What Is This Study About? This study will test whether losartan, a medication often used for high blood pressure, can help hearts recover better after aortic valve replacement surgery. The researchers will compare two groups of patients: * One group will take losartan (50 mg per day) after surgery. * The other group will take a placebo (a pill with no active medication). By comparing these two groups, the study will determine whether losartan helps the heart shrink back to a normal size faster and function better after surgery. How Will the Study Work? Who? 60 patients with severe AR who are having aortic valve replacement surgery. How? Patients will be randomly placed into one of the two groups (losartan or placebo). For how long? Patients will be followed for one year after surgery. What Will Be Measured? Doctors will check patients four times: before surgery, and 1 month, 3 months, and 12 months after surgery. At each visit, the investigators will measure: * NT-proBNP levels: A blood test that tells us how much strain the heart is under. Lower levels mean the heart is recovering well. * Echocardiogram: An ultrasound of the heart to check its size and function. * 6-minute walk test: To see if patients feel stronger and can exercise better. * Quality of life survey: To understand how patients feel physically and emotionally. * Kidney function and electrolyte levels: To check for medication side effects. Why Is This Study Exciting? This is the first study to test whether a medication can help the heart heal better after valve surgery. If losartan proves beneficial, it could change how doctors treat patients after surgery and lead to better recovery, stronger hearts, and healthier lives. Many people with aortic regurgitation have to wait until their symptoms get worse before patients can have surgery. If this study finds that medication can speed up healing, it could help doctors treat valve disease more effectively and improve long-term outcomes for patients. What Happens Next? If losartan is found to be helpful, this study could lead to larger research trials and, eventually, new treatment guidelines for people who have had aortic valve surgery. If it doesn't help, doctors will know not to prescribe it unnecessarily, preventing unnecessary side effects and costs for patients. Either way, the results will help improve care for people with heart valve disease. By participating in this study, patients are helping researchers discover new ways to improve heart health and recovery after surgery.

Participants needed: 60
Trial details
Phase: Phase 4Age: 18-85Biological sex: AllType: InterventionalSponsor: Vitor Emer Egypto RosaUpdated: Aug 1, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years; [+2]

Those who underwent cardiac surgery in the context of cardiogenic shock or infec... [+7]

Status: Not yet recruiting

Feasibility Study to Support Cardiorenal Function in Acute Decompensated Heart Failure With Diuretic Resistance

Evaluation of the safety and efficacy of the ModulHeart System in patients hospitalized with acute decompensated heart failure (ADHF) and diuretic resistance

Participants needed: 5
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: Puzzle Medical Devices Inc.Updated: Jun 17, 2024Locations: 5
Eligibility criteria

Admitted to the hospital with a primary diagnosis of ADHF [+10]

ADHF related to acute secondary disease (i.e., infection or acute coronary syndr... [+35]

Status: Recruiting

Diuretics vs. Afterload Reduction for Treatment of HeartLogic Alerts

The DART-HA study is a single-center, open label, trial intended to evaluate the clinical efficacy of standard treatment options for congestive heart failure (observation, diuretic or afterload reduction therapy) in patients without new symptoms who have developed abnormalities of the HeartLogic heart failure diagnostic feature.

Participants needed: 80
Trial details
Phase: Phase 4Age: 19+Biological sex: AllType: InterventionalSponsor: Heart Center Research, LLCUpdated: Jan 29, 2024Locations: 1
Eligibility criteria

Boston Scientific device with HeartLogic enabled [+8]

Glomerular filtration rate <25 mL/min who are non-responsive to diuretic therapy... [+9]