Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06652087

Rifaximin and Cardiac Function in Patients with Heart Failure with Preserved Ejection Fraction

Led by I.M. Sechenov First Moscow State Medical University · Updated on 2024-10-22

40

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Single-center, double-blind, randomized, controlled intervention study of the effect of correction of bacterial overgrowth syndrome in the small intestine (SIBO) on cardiac function in patients with heart failure with preserved ejection fraction (HFpEF) (SIBO-HFpEF). The aim of the study is to evaluate the efficacy and safety of rifaximin in patients with HFpEF and SIBO.

CONDITIONS

Official Title

Rifaximin and Cardiac Function in Patients with Heart Failure with Preserved Ejection Fraction

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent to participate in the study
  • Adults aged 18 to 80 years
  • Body mass index of 25 kg/m2 or higher
  • Diagnosed with heart failure with preserved ejection fraction (HFpEF), including symptoms or signs of heart failure, left ventricular ejection fraction of 50% or higher, increased natriuretic peptide levels (NTproBNP 6 125 pg/mL), and at least one additional heart-related criterion such as left ventricular hypertrophy, left atrial enlargement, or diastolic dysfunction
Not Eligible

You will not qualify if you...

  • Patient refusal to continue participation in the study
  • Presence of severe diseases or conditions making monitoring difficult or data interpretation unreliable, such as gastrointestinal bleeding or recent myocardial infarction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Moscow

Moscow, Russia

Actively Recruiting

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Research Team

K

Konstantin Ivashkin

CONTACT

E

Elena Bueverova

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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