Heart Failure, Diastolic

14

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

Condition / disease
Location
Status: Recruiting

A Randomised, Controlled Trial of a Low-energy Diet for Improving Functional Status in Heart Failure With PRESERVED Ejection Fraction Preserved Ejection Fraction

Heart failure with preserved ejection fraction (HFpEF) is a common and serious complication of obesity and type 2 diabetes (T2D). HFpEF occurs when the heart muscle unable to relax efficiently to pump the blood around the body. This leads to fluid build-up, breathlessness and inability to tolerate physical exertion. People who develop HFpEF do less well because treatment options are limited. Pilot data in patients with obesity and diabetes and a small number of patients with HFpEF have shown improvements in exercise capacity and reversal of changes in the heart and blood vessels. This study will assess if this is achievable in a multi-ethnic cohort of patients with established HFpEF. A total of 63 adults will be invited and allocate by chance into two groups: 1) 12-weeks of a low calorie diet or 2) Standard care and health advice on how to lose weight followed by the option to have the low calorie diet after 12-weeks. The study will determine if weight loss over 12 weeks can improve heart function, symptoms and ability to exercise. Additionally, participants' views on changing their diet and how this has impacted their symptoms will be sought during the study in an optional interview. This will help guide treatments planning in the future to get maximum benefits, and to individualize support to patients from different cultural backgrounds.

Participants needed: 63
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University of LeicesterUpdated: Jun 25, 2026Locations: 3
Eligibility criteria

Established clinical diagnosis of heart failure with preserved ejection fraction... [+3]

Inability to walk/undertake 6-minute walk test [+16]

Status: Not yet recruiting

A Study of LY3971297 in Participants With Heart Failure

The main purpose of this study is to assess how well LY3971297 is tolerated and what side effects may occur in participants with heart failure with preserved ejection fraction (HFpEF) and participants with heart failure with reduced ejection fraction (HFrEF). Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. For each participant, the study will last about 2 months and will include 1 inpatient visit lasting approximately 4 days and 5 outpatient visits.

Participants needed: 90
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Eli Lilly and CompanyUpdated: Jun 16, 2026Locations: 10
Eligibility criteria

Are diagnosed with chronic heart failure with New York Heart Association Class I... [+16]

Have known allergies to related compounds of LY3971297 or any components of the... [+29]

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: Not yet recruiting

Incretin Therapies in Obesity-related HFpEF

The central hypothesis to be tested is that patients with obesity and heart failure with preserved ejection fraction (HFpEF) prescribed tirzepatide will demonstrate reductions in measured plasma volume. In conjunction with state-of-the-art body composition analysis and measures of adipokines, this will establish an important mechanism of clinical benefit and inform disease pathophysiology. To accomplish this, this study will perform a 15-month prospective cohort study in 50 patients with obesity and HFpEF who clinically qualify for treatment with tirzepatide. The investigators will serially measure plasma volume and body composition with quantitative magnetic resonance to determine changes over time with tirzepatide treatment.

Participants needed: 50
Trial details
Phase: Phase 4Age: 40+Biological sex: AllType: InterventionalSponsor: Columbia UniversityUpdated: May 4, 2026
Eligibility criteria

Diagnosis of heart failure (HF) per the ACC/AHA guidelines with NYHA class II-II... [+4]

Acute decompensated HF within 4 weeks of screening [+10]

Status: Not yet recruiting

Data-Driven Phenotyping in Heart Failure With Preserved Ejection Fraction

The goal of this observational study is to learn how people with Heart Failure with Preserved Ejection Fraction (HFpEF) can be grouped into different "phenotypes" based on their clinical information. The researchers want to understand whether these groups have different health profiles and different responses during a cardiopulmonary exercise test (CPET). The main questions this study aims to answer are: * Can clinical data be used to identify meaningful HFpEF phenotypes? * Do these phenotypes match well-known HFpEF scores, such as the H2FPEF and Heart Failure Association Pre-test Assessment, Echocardiography and Natriuretic Peptide (HFA-PEFF) scores? * Do people in different phenotypes show different results on a CPET? Participants will: * Have their past clinical records reviewed if they were diagnosed with HFpEF at the Local Health Unit of the Leiria Region (ULS RL); * A smaller group will attend one visit to complete a CPET, which measures how the heart, lungs and muscles respond during exercise. This study includes adults aged 18 years or older who have HFpEF. The study does not involve any new treatments or experimental drugs.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Instituto Politécnico de LeiriaUpdated: Feb 24, 2026Locations: 2
Eligibility criteria

Age ≥18 years; [+6]

Incomplete or inadequate medical records preventing full data extraction. [+2]

Status: Recruiting

Associations Between the Microbiome, Skeletal Muscle Perfusion, and Fitness Status

The purpose of the study is to determine associations between fitness status, bacteria in the mouth, and the blood flow to muscle. This study is trying to find out if fitness status impacts the bacteria that are present in the oral microbiome (environment in the mouth) or the ability of the body to send blood to the skeletal muscle. Participants will complete all or some of the following: * A mouth swab to assess the bacteria in their mouths. * Produce a saliva sample into a tube. * Cycle on a bike until you reach maximum effort. * Undergo blood draws * Wear a 24-hour non-invasive device that monitors blood pressure. * Drink 70mL (1/3 of a cup) of concentrated beetroot juice once

Participants needed: 70
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of VirginiaUpdated: Dec 24, 2025Locations: 1
Eligibility criteria

Subjects must be able to communicate meaningfully with the investigator and must... [+1]

Oral antibiotic use within previous four weeks [+9]

Status: Recruiting

Comparative Efficacy and Safety of Acetazolamide Versus Metolazone as an Adjunct to Standard Therapy in Patients With Acute Decompensated Heart Failure

This clinical trial aims to compare the efficacy and safety of acetazolamide versus metolazone as adjunctive treatments to standard therapy in patients with acute decompensated heart failure (ADHF). ADHF is a life-threatening condition, and current treatments often involve loop diuretics to alleviate volume overload. This study will assess the added benefit of acetazolamide and metolazone in improving decongestion, reducing hospital stays, and preventing complications such as renal dysfunction or electrolyte imbalances. Participants will be randomized to receive either acetazolamide or metolazone in addition to standard diuretic therapy. The trial will evaluate primary outcomes including successful decongestion, in-hospital mortality, and length of hospital stay, with secondary outcomes focusing on renal function, electrolyte disturbances, and overall safety. The study is conducted at Bahawal Victoria Hospital, Bahawalpur, and aims to provide valuable insights into the management of ADHF, especially in the Pakistani population.

Participants needed: 320
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Health Sciences LahoreUpdated: Oct 3, 2025Locations: 1
Eligibility criteria

Aged 18 years or older. [+5]

Previous use of acetazolamide or metolazone prior to the study period. [+7]

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

Multiple-biomarker Approach for Individualized Treatment of Heart Failure with Preserved Ejection Fraction

The primary objective is to investigate the association between temporal evolutions of blood biomarkers and clinical adverse events, in order to produce a dynamic, individual, and accurate prediction model for patients with HFpEF. Moreover several secondary objectives will be investigated.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Erasmus Medical CenterUpdated: Jan 21, 2025Locations: 6
Eligibility criteria

Age of 18 years or older [+2]

History of LVEF ≤40% [+9]

Status: Recruiting

Prevalence and Prediction of ATTR in Ambulatory Patients With HFpEF

Recent studies have shown that transthyretin amyloidosis (ATTR) can sometimes cause a type of heart failure where the pumping function of the heart is normal, also known as Heart Failure with Preserved Ejection Fraction (HFpEF) or diastolic heart failure. In this single center diagnostic study, we will evaluate for ATTR in patients with HFpEF in order to to determine how frequently this occurs and how we can predict which heart failure patients may have TTR amyloidosis. Our goal is to identify amyloidosis in heart failure patients earlier so that they can start treatment.

Participants needed: 515
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Dec 9, 2024Locations: 1
Eligibility criteria

Patients with a confirmed diagnosis of HFpEF. [+1]

End stage chronic kidney disease on dialysis (CKD stage 5 as defined as eGFR <15... [+5]

Status: Recruiting

Value of Intense Phenotyping in Heart Failure With Preserved Ejection Fraction

Heart failure (HF) with a left ventricular ejection fraction (LVEF) \>0.40 is a large medical problem, for which no drug or device has a recommendation in current HF guidelines. The prevalence of mortality and HF hospitalizations in HF with LVEF \>0.40 is high, but the identification of predictors for increased risk of mortality and HF hospitalizations in this patient category remains difficult. The hypothesis of this study is that the risk of all-cause mortality and HF hospitalizations can be measured by clinical factors, imaging parameters and circulating biomarkers, and that these factors can be used in a risk profile

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Medical Center GroningenUpdated: May 16, 2024Locations: 1
Eligibility criteria

Age >18 years [+8]

Patients unwilling or unable to sign informed consent [+6]

Status: Recruiting

Modulation of SERCA2a of Intra-myocytic Calcium Trafficking in Heart Failure With Preserved Ejection Fraction

The goal of this clinical trial is to test an experimental gene therapy in participants with heart failure with preserved ejection fraction, also known as diastolic heart failure. The main questions it aims to answer are: * safety and tolerability of the gene therapy; and * whether the gene therapy helps the heart ventricles relax during filling. Participants will undergo a one-time infusion of the gene therapy in the cardiac catheterization laboratory and then be followed for safety and effects on left-sided filling pressures while exercising. The first year will have multiple in-person visits followed by 4 years of biannual phone calls.

Participants needed: 10
Trial details
Phase: Phase 1Age: 50+Biological sex: AllType: InterventionalSponsor: Sardocor Corp.Updated: Sep 29, 2023Locations: 2
Eligibility criteria

Willing and able to provide informed consent [+6]

NYHA class IV [+11]

Status: Recruiting

Multimodality Imaging in the Screening, Diagnosis and Risk StratifictiON of HFpEF

The incidence of Heart failure with preserved ejection fraction (HFpEF) in Heart failure patients increases rapidly. However, the current clinical awareness is insufficient, and the cardiac structural and functional injury are not well understood. It is difficult to recognize the subclinical changes of the cardiac in the early stage with conventional imaging techniques, and it is common to ignore the existence of the clinical alterations. This study aimed to investigate the cardiac features, early diagnosis and risk factors of HFpEF patients, based on the multi-modal (Magnetic resonance imaging- nuclear medicine imaging- echocardiography) imaging, combined with large data and artificial intelligence. This study will provide deep insights into the HFpEF derived from different causes.

Participants needed: 430
Trial details
Biological sex: AllType: ObservationalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Nov 8, 2022Locations: 1
Eligibility criteria

left ventricular ejection fraction (LVEF)≥50%; [+3]

Special types of cardiomyopathy, including hypertrophic cardiomyopathy, restrict... [+5]

Status: Recruiting

Diagnosis and OutcoMes evaluAtIoN of Multicenter Patients With HFpEF Using Multimodality Imaging

The incidence of Heart failure with preserved ejection fraction (HFpEF) in Heart failure patients increases rapidly. However, the current clinical awareness is insufficient, and the cardiac structural and functional injury are not well understood. It is difficult to recognize the subclinical changes of the cardiac in the early stage with conventional imaging techniques, and it is common to ignore the existence of the clinical alterations. This study aimed to investigate the cardiac features, early diagnosis and risk factors of HFpEF patients, based on the multi-modality (Magnetic resonance imaging- nuclear medicine imaging- echocardiography) imaging and multicenter study, combined with large data and artificial intelligence. This study will provide deep insights into the HFpEF in multicenter population.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Apr 18, 2022Locations: 1Duration: 8 Years
Eligibility criteria

left ventricular ejection fraction (LVEF)≥50%; [+3]

Special types of cardiomyopathy, including hypertrophic cardiomyopathy, restrict... [+5]