Registry for Patients With and Without Heart Failure
Official title: Preserved vs. Reduced Ejection Fraction Biomarker Registry and Precision Medicine Database for Ambulatory Heart Failure Patients (PREFER-HF) Study
Run by Massachusetts General Hospital · NCT03480633 · Data updated 2026-11-12
This study is looking to understand different types of heart failure by gathering health information from people aged 18 and older, both with and without the condition, to improve treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | Massachusetts General Hospital Academic / other |
| Locations | 1 site (Boston, Massachusetts) |
| Status | Recruiting |
| Started | April 7, 2016 |
| Main results expected | October 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | August 31, 2026 |
| Trial ID | NCT03480633 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with a history of clinical symptoms consistent with heart failure.
✕Probably not a fit
Patients with end-stage renal disease on dialysis may not receive any benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational registry aims to comprehensively examine clinical characteristics, proteomic, metabolomic, genomic, and imaging data to understand the development and progression of different types of heart failure. Patients aged 18 and older, both with and without heart failure, will be enrolled to evaluate distinct heart failure phenotypes and cardiomyopathies, including amyloidosis. The study will collect baseline and one-year follow-up data, including blood samples and clinical outcomes, to optimize precision medicine in heart failure treatment.
Why it matters
Potential benefit: If successful, this study could lead to more personalized and effective treatments for patients with heart failure.
How similar studies have gone: Other studies have shown success in using similar approaches to improve understanding and treatment of heart failure, indicating this study builds on established methodologies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria for patients with HF: * 18 years and older * History of clinical symptoms consistent with HF and at least one of the following supporting evidence of HF: * NT-proBNP \> 125 pg/mL * BNP \> 35 pg/mL * Capillary wedge pressure ≥ 15 mmHg on right heart catheterization or CI \<2.8 L/min/m2 * LVEDP ≥ 15 mmHg * Radiographic evidence of pulmonary edema * Improvement in symptoms with diuretic initiation of increase * CPET evidence of cardiac etiology of symptoms HFpEF: LVEF ≥ 50% HFrEF: LVEF \<50% Exclusion criteria (for all patients, including both those with HFpEF and HFrEF): \- End stage renal disease on dialysis
Where it's running
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Massachusetts General Hospital
Boston, Massachusetts, United States Recruiting
Study contacts
- Principal investigator: Hanna Gaggin, MD, MPH — Massachusetts General Hospital
- Study coordinator: Abbie Macher, BS
- Email: ajmacher@mgh.harvard.edu
- Phone: 617-643-6328
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.