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NCT05093959CompletedPhase 2

Metformin for Older Patients With Heart Failure With Preserved Ejection Fraction

Source: ClinicalTrials.gov · Last updated 10 Jun 2026

Brief summary (registry, in English)

Met-PEF will be a randomized, double-blind, placebo-controlled trial to examine the effects of 20 weeks of 1500 mg/day of metformin on physical function, quality of life (QOL), microbiome diversity, leaky gut, and systemic inflammation in patients with 86 older patients with heart failure with preserved ejection fraction (HFpEF).

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
86 (actual)
First submitted
22 Oct 2021
Start date
4 Jan 2022
Primary completion date
18 Dec 2025
Lead sponsor
Wake Forest University Health Sciences
NCT number
NCT05093959

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 86
  • From 4 Jan 2022 to the primary completion date, 18 Dec 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of treatment with metformin or other anti-diabetic drug intended to treat diabetes

Other illness

  • Uncontrolled hypertension (systolic blood pressure \[SPB\]\>200 mmHg or diastolic blood pressure \[DBP\]\>100 mmHg at rest)
  • Known valvular heart disease, infiltrative cardiomyopathy, or hypertrophic obstructive cardiomyopathy with active obstruction as the primary etiology of HF
  • Evidence of significant chronic obstructive pulmonary disease (COPD) defined as either: a. On continuous home oxygen therapy for COPD; b. Hospitalization for COPD in last 6 months
  • Any condition that in the judgement of the investigator precludes participation in study or study procedures such as significant dementia, mobility impairment, uncontrolled psychiatric disease, etc.
  • Current or recent cancer, or chemotherapy/radiation treatment
  • Exclusions for microbiome testing: a. Antibiotics use within last 30 days; b. Diarrhea and/or vomiting within last 30 days; c. Surgery related to gut in last 6 months; d. Inflammatory bowel disease (such as Crohn's disease or ulcerative colitis), or irritable bowel syndrome

Lab values

  • Significant anemia (\<9.5 g hemoglobin \[Hb\]) (eligibility will be determined by complete blood count)
  • Significant renal insufficiency (estimated glomerular filtration rate \[eGFR\] \<45 ml/min/1.73 m2) (eligibility will be determined by comprehensive metabolic panel)
  • Type 2 diabetes, or HbA1c\>6.5

Other

  • Body mass index (BMI) \<25.0
  • Uncontrolled dysrhythmia
  • Acute or chronic metabolic acidosis
  • Low vitamin B12 (\<232 pg/mL)
  • Alcohol abuse (\>14 drinks/week)
  • Pregnancy-women of child-bearing potential are excluded from participation in this study.
  • A treadmill exercise test revealing: a. Evidence of significant ischemia; b. Electrocardiogram: 1mm flat ST depression; c. Stopped exercising due to chest or leg claudication or any reason other than exhaustion/fatigue/dyspnea; d. Exercise SBP \> 240 mmHg, DBP \> 110 mmHg ; e. Unstable hemodynamics or rhythm; f. Unwilling or unable to complete adequate exercise test
  • Plans to leave area within 1 year
  • Currently participating in other investigational study
  • Refuses informed consent

Who the study is looking for

  • Heart failure with preserved ejection fraction (HFpEF) will be defined in accord with the American College of Cardiology/American Heart Association 2013 guidelines statement on Management of heart failure and as previously described. The 4 key inclusion criteria for HFpEF include: 1) clinical signs and symptoms as scored by National Health and Nutrition Examination Survey (NHANES)-HF Clinical Score ≥3 and the Rich Criteria; 2) a normal left ventricular (LV) ejection fraction (≥50%) by echocardiography; 3) LV diastolic dysfunction \> grade 1 (American Society of Echocardiography Recommendations); 4) no evidence of significant ischemic, valvular, pulmonary or other medical disorder to account for their symptoms.
  • Age ≥60
  • Stable HF symptoms and medications for ≥3 weeks
  • Final eligibility will be based upon all information available at the conclusion of the baseline visits tests, including review of hospital and outpatient records, history, physical examination, echocardiogram, and familiarization/screening exercise test by a board-certified investigator cardiologist who have extensive experience in heart failure investigations in older persons with HFpEF

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Atrium Health Sanger Heart and Vascular Clinic Institute
Coordinator of this site? Confirm its status
CharlotteUnited StatesUnknown status
Wake Forest School of Medicine
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.