Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06573892

The Gut Microbiome in Chronic Heart Failure

Led by Nazarbayev University · Updated on 2024-08-27

90

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

there are numerous studies, most of which are predominantly associative in nature, investigating the association between the gut microbiota and various pathologies. However, to establish a causal relationship between microbiome composition and chronic heart failure (HF), clinical studies are needed, particularly using probiotics that can modify the composition and function of the gut microbiota. Examining their effects on HF can help understand which specific changes are associated with improvement or slowing the progression of the disease. The gut microbiome plays an important role in regulating the immune system and inflammatory processes. Investigating the impact of probiotics on these mechanisms may reveal their potential anti-inflammatory and immunomodulatory properties, which can be beneficial for controlling the inflammation characteristic of HF. Additionally, studying the interaction of probiotics with other medications, such as antihypertensive and diuretic agents, can be crucial for optimizing pharmacotherapy in HF patients. Confirming the role of the gut microbiota in the pathogenesis of HF and further developing probiotic therapy may lead to improved prognosis and treatment outcomes for HF patients. Overall, conducting a clinical study using probiotics in HF has the potential to expand our knowledge of the role of the gut microbiota in this disease and lay the groundwork for the development of new treatment strategies.

CONDITIONS

Official Title

The Gut Microbiome in Chronic Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Living in the city of Astana or surrounding Akmola region
  • Diagnosed with heart failure according to international guidelines
  • Heart failure classified as NYHA Class I-IV or ACC/AHA Stage A-C
  • Clinically stable with optimized heart failure medication for at least 4 weeks
  • Willingness to participate in the study
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Declines required diagnostic procedures
  • Terminal heart failure (ACC/AHA Stage D)
  • Major heart or other surgeries within 3 months before enrollment
  • Use of antibiotics, cytostatic therapy, or probiotics/prebiotics within 1 month before baseline
  • Presence of cancer or autoimmune diseases
  • Current acute illness or infection
  • Intolerance to probiotics
  • Other medical, social, or psychological conditions limiting study participation or follow-up

AI-Screening

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Trial Site Locations

Total: 1 location

1

Heart Center

Astana, Kazakhstan, 010000

Actively Recruiting

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Research Team

A

Almagul Kushugulova

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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