A study testing whether a GLP-1 and GIP medicine, tirzepatide, can help people with diastolic heart failure lose weight.

Recruiting now. Registry record last updated August 24, 2026.

Who can join
Adults 40+, have diastolic heart failure, BMI 30+.
What you take
Tirzepatide, given as part of the study. Check ClinicalTrials.gov for this trial's study groups, including any placebo or comparison medicine.
How long it lasts
The full study runs about 4 years.
What you get
Costs vary by study. Ask the study team what this one covers, including the study medicine, visits and travel, before you sign the consent form.
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Phase Phase 4Sponsor Columbia UniversityDrug tirzepatideClass GLP-1/GIPSites 1 USEnrollment target 50

What this study is for

Primary condition: Heart Failure, Diastolic. Also studied in: Heart Failure With Preserved Ejection Fraction, Obesity.

Full scientific study title: Incretin Therapies in Obesity-related HFpEF.

Who can join

Age40 and upSexAnyBMI30 or higher

Adults 40+, have diastolic heart failure, BMI 30+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • Diagnosis of heart failure (HF) per the ACC/AHA guidelines with NYHA class II-III symptoms
  • Left ventricular ejection fraction \>= 45% within 6 months of recruitment
  • At least one of the following: elevated N-terminal pro- B-type natriuretic peptide (NT-proBNP) \>=200 pg/ml (\>=600 pg/ml with concurrent atrial fibrillation), evidence of structural heart disease (left atrial (LA) enlargement with LA volume index \>29 mL/m2 or LA diameter \>=40 mm in males/\>38= mm in females), elevated filling pressures (resting wedge \>15 mmHg or exercise wedge \>25 mmHg, lateral E/e' ratio \>12 or septal E/e' \> 15)
  • Body mass index (BMI) \>30 kg/m2
  • Stable doses of HF medications within 4 weeks of screening with optimal volume control in the opinion of the investigator.

Key exclusion criteria

  • Acute decompensated HF within 4 weeks of screening
  • Major cardiovascular event within 90 days of screening (myocardial infarction, stroke)
  • Alternate cause of HFpEF such as cardiac amyloidosis, infiltrative cardiomyopathy, hypertrophic cardiomyopathy, severe valvular disease
  • Estimated glomerular fibrilation rate (EGFR) \<15 ml/min/1.73m2 or dialysis dependence
  • Poorly controlled diabetes (A1c \> 9.5%) OR any type 1 diabetes mellitis

Where this trial is enrolling

This trial has 1 sites across 1 state. Contact a site coordinator directly to start screening.

New York1 site
  • Columbia University Irving Medical Center (CUIMC) / NewYork Presbyterian Hospital (NYP)
    New York, New York

Timeline

Started enrolling: August 7, 2026. Expected completion: April 2030. Last updated on ClinicalTrials.gov: August 24, 2026.

Official source

Every Monday we check this trial against ClinicalTrials.gov, the federal registry for clinical research. Last checked September 4, 2026. Confirm the current status there before you contact a site:

View on ClinicalTrials.gov →

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