Heart Failure Clinical Trials in Cincinnati, Ohio
18 studies are recruiting for heart failure in Cincinnati, Ohio right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Phase III Study Investigating Heart Failure and Cardiovascular Death With Baxdrostat in Combination With Dapagliflozin
Participants include men and women ≥ 40 years of age with T2DM, established CV disease, a history of HTN with an SBP of at least 130 mmHg at screening, who meet the predefined serum potassium level, and with at least one additional risk factor for HF. The study will include an optional pre-screenin…
- Stage
- Phase 3
- Ages
- 40 and older
- Site
- Research Site, Cincinnati, Ohio
- Locations
- 957 in total
- Run by
- AstraZeneca
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Barostim-Enabled NEurohormonal Intervention For Improving Treatment of Heart Failure
The purpose of BENEFIT-HF is to demonstrate the safety and effectiveness of Baroreflex Activation Therapy (BAT) with the Barostim System in participants with heart failure, defined as NYHA Functional Class II or III, LVEF < 50% and NT-proBNP < 5,000 pg/mL despite being treated with Guideline-Direct…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Christ Hospital, Cincinnati, Ohio
- Locations
- 11 in total
- Run by
- CVRx, Inc.
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A Study to Determine the Efficacy and Safety of Finerenone on Morbidity and Mortality Among Hospitalized Heart Failure Patients
Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients hospitalized with acute decompensated heart failure (HF) and mildly reduced or preserved left ventricular ejection fraction.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Cincinnati, OH Investigative Site 10088, Cincinnati, Ohio
- Locations
- 356 in total
- Run by
- Colorado Prevention Center
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Investigation of the BrioVAD System for the Treatment of Left Ventricular Heart Failure
The goal of this study is to evaluate the safety and efficacy of the BrioVAD System by demonstrating non-inferiority to the HeartMate 3 Left Ventricular Assist System when used for the treatment of advanced, refractory, left ventricular heart failure.
- Stage
- Not phased
- Ages
- 18 to 100
- Site
- The Christ Hospital - Cincinnati, Cincinnati, Ohio
- Locations
- 47 in total
- Run by
- BrioHealth Solutions, Inc.
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Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Left Ventricular Systolic Dysfunction (MK-1242-036)
This study aims to compare the efficacy of vericiguat versus placebo on change in n-terminal pro-brain natriuretic peptide (NTproBNP) from baseline to Week 16 of the Base Period. The primary hypothesis is that vericiguat is superior to placebo in reducing NT-proBNP at Week 16 of the Base Period.
- Stage
- Phase 2
- Ages
- 0 to 17
- Site
- Cincinnati Children's Hospital Medical Center ( Site 0034), Cincinnati, Ohio
- Locations
- 109 in total
- Run by
- Merck Sharp & Dohme LLC
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Study With Omecamtiv Mecarbil (CK-1827452) to Treat Chronic Heart Failure With Severely Reduced Ejection Fraction
The purpose of this study is to find out if the investigational drug called omecamtiv mecarbil can reduce the risk of the effects of heart failure, like hospitalization, transplantation, or death in patients with heart failure and severely reduced ejection fraction.
- Stage
- Phase 3
- Ages
- 18 to 85
- Site
- The Lindner Research Center at the Christ Hospital, Cincinnati, Ohio
- Locations
- 205 in total
- Run by
- Cytokinetics
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NORM-HF Pivotal Study
This is an international, multi-center, prospective, randomized, open-label blinded endpoint study designed to demonstrate that use of the FIRE1 NORM™ System in the management of New York Heart Association Class II/III HF patients is superior for reducing the combined endpoint of worsening HF event…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Christ Hospital Lindner, Cincinnati, Ohio
- Locations
- 9 in total
- Run by
- Foundry Innovation & Research 1, Limited (FIRE1)
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Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)
The study investigators are interested in learning more about how drugs, that are given to children by their health care provider, act in the bodies of children and young adults in hopes to find the most safe and effective dose for children. The primary objective of this study is to evaluate the PK…
- Stage
- Not phased
- Ages
- 0 to 20
- Site
- Cincinnati Childrens Hospital Medical Center, Cincinnati, Ohio
- Locations
- 52 in total
- Run by
- Duke University
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Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products
The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.
- Stage
- Not phased
- Ages
- Any age
- Site
- Research site, Cincinnati, Ohio
- Locations
- 333 in total
- Run by
- Medtronic
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A Research Study to Look at How Well NNC0487-0111 Works Compared to Placebo in People With Heart Failure and Obesity
This study is being done to look at the safety and effect of NNC0487-0111 in people with Heart Failure with preserved Ejection Fraction (HFpEF) or Heart Failure with mildly reduced Ejection Fraction (HFmrEF) and excess body weight when compared to placebo. The purpose of this clinical study is to f…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Lindner Center,Christ Hospital, Cincinnati, Ohio
- Locations
- 838 in total
- Run by
- Novo Nordisk A/S
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Assessment of CCM in HF With Higher Ejection Fraction
The AIM HIGHer Clinical Trial will evaluate the safety and efficacy of Cardiac Contractility Modulation (CCM) therapy in patients with heart failure with LVEF ≥40% and ≤70%.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- TriHealth Bethesda, Cincinnati, Ohio
- Locations
- 105 in total
- Run by
- Impulse Dynamics
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A Study to Evaluate Finerenone on Clinical Efficacy and Safety in Patients With Heart Failure Who Are Intolerant or Not Eligible for Treatment With Steroidal Mineralocorticoid Receptor Antagonists
Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients with heart failure and reduced ejection fraction (HFrEF) who are intolerant or ineligible to receive treatment with steroidal mineralocorticoid receptor antagonists (sMRA).
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- FIN- 10112, Cincinnati, OH, Cincinnati, Ohio
- Locations
- 176 in total
- Run by
- Colorado Prevention Center
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PROACTIVE-HF-2 Trial Heart Failure NYHA Class II and III
This is a prospective, multi-center, open label, randomized control clinical trial evaluating the safety and efficacy of the Cordella™ Pulmonary Artery Sensor System in NYHA Class II-III Heart Failure Patients (PROACTIVE-HF-2 Trial). The study contains of 5 arms: NYHA II Cohort - To demonstrate saf…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Christ Hospital- Cincinnati, Cincinnati, Ohio
- Locations
- 48 in total
- Run by
- Endotronix, Inc.
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Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients With Advancing Heart Failure
The purpose of TEAM-HF IDE clinical trial is to evaluate safety and effectiveness of the HeartMate 3 LVAS compared to guideline directed medical therapy (GDMT) in a population of ambulatory advanced heart failure patients who are not dependent on intravenous inotrope.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Christ Hospital, Cincinnati, Ohio
- Locations
- 68 in total
- Run by
- Abbott Medical Devices
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The EMPOWER Trial - The Carillon Mitral Contour System® in Treating Heart Failure With FMR
The objective of this prospective, randomized, double- blinded (patient and assessors), sham-controlled clinical trial is to assess the safety and efficacy of the CMCS in treating heart failure with functional regurgitation (FMR).
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Lindner Research Center at the Christ Hospital, Cincinnati, Ohio
- Locations
- 92 in total
- Run by
- Cardiac Dimensions, Inc.
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Left vs Left Randomized Clinical Trial
The investigators aim to prospectively test the comparative effectiveness of His or Left bundle branch pacing in relation to patient centered outcomes (quality of life, physical activity, heart failure hospitalization, mortality) and comparative safety in relation to device-related complications an…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Christ Hospital, Cincinnati, Ohio
- Locations
- 71 in total
- Run by
- Baylor College of Medicine
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AN INTERNATIONAL, OBSERVATIONAL, BLINDED STUDY TO ASSESS THE PERFORMANCE OF THE CORDIO HEARO SYSTEM
Study Design: This is an international, multicenter, observational, non-interventional, prospective, blinded, single-arm, two-period study, to collect patient utterances that will be retrospectively analyzed to determine the sensitivity and UPNR of the HearO system.
- Stage
- Not phased
- Ages
- 22 and older
- Site
- The Lindner Research Center at The Christ Hospital, Cincinnati, Ohio
- Locations
- 45 in total
- Run by
- Cordio Medical
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BiVACOR® Total Artificial Heart Early Feasibility Study
The purpose of this study is to assess the feasibility of using the BiVACOR Total Artificial Heart (TAH) System to support adult patients with severe biventricular heart failure, or univentricular heart failure in which left ventricular assist device (LVAD) support is not recommended, who require m…
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- The Christ Hospital, Cincinnati, Ohio
- Locations
- 4 in total
- Run by
- BiVACOR Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
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