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Urolihin A in heart Failure

Evaluation of urolithin A efficacy in heart failure patients with reduced ejection fraction

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210216050375N1
Enrollment
10
Registered
2021-02-27
Start date
2021-08-23
Completion date
Unknown
Last updated
2021-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

heart failure with reduced ejection fraction. Heart failure

Interventions

Intervention 1: Intervention group: Patients will receive 250 mg Urolithin A BID for one month. Intervention 2: Control group: placebo pills BID for one month.

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: Male Between the ages 25 to 85 years Left ventricular ejection fraction equal or lower than 40% New York Heart Association functional class equal or greater than II Received standard treatment of heart failure (including Angiotensin-converting enzyme 2 inhibitors or Angiotensin II receptor inhibitors and beta blockers) for at least 2 weeks Signed informed consent

Exclusion criteria

Exclusion criteria: History of myocardial infarction during the 8 past weeks History of any malignant disease Renal failure (eGFR lower than 20 ml/1.73 m2/min) hepatic disorder (aminotransferase > 2x upper limit of normal) Extensive heart surgery or angioplasty during the past 30 days Allergy and/or hypersensitivity to specific drugs or substances related to drug used in this clinical trial uncontrolled high blood pressure (Systolic blood pressure higher than 180 mmHg and diastolic blood pressure higher than 100 mmHg)

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction. Timepoint: Before and 1 month after intervention. Method of measurement: Echocardiography.

Secondary

MeasureTime frame
N-terminal pro b-type natriuretic peptide (NTproBNP). Timepoint: Before and 1 month after intervention. Method of measurement: Evaluation in serum by using a commercially available kit.;NYHA functional class. Timepoint: Before and 1 month after intervention. Method of measurement: Evaluation of symptoms by clinician.;Serum cardiac troponin. Timepoint: Before and 1 month after intervention. Method of measurement: Evaluation in serum by using a commercially available kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMilad Iranshahi

Mashhad University of Medical Sciences

iranshahiml@mums.ac.ir009831801253

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026