Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Heart Center
Astana, Kazakhstan, 010000
Actively Recruiting
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
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here