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The Influence of Probiotics on Metabolome and Heart Rate Variability in Heart Failure of Structure Heart Disease

NCT06872320 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-03-28
Last updated
2025-07-22

Condition(s) studied

Congenital Heart DiseaseDysbiosisMalnutrition, ChildProbioticsMetabolome

Investigational drug(s) / intervention(s)

Lactobacillus Rhamnosus →Placebo

Lactobacillus Rhamnosus: Lactobacillus Rhamnosus (Lactobacillus Rhamnosus, MoProbi-LR Capsules, Drug permit license 052531); Age \< 2 years old: 1/2 capsule once daily for 24 weeks per oral Age ≥ 2 years old: 1 capsule once daily for 24 weeks per oral

Placebo: Maltodextrin comparable in color. Age \< 2 years old: 1/2 capsule once daily for 24 weeks per oral Age ≥ 2 years old: 1 capsule once daily for 24 weeks per oral

Study summary

Poor body weight gain and failure to thrive is a very common condition in patients with congenital heart disease (CHD) with advanced HF and/or cyanosis, which are considered a predictor of morbidity and complicate the prognosis of CHD. Studies have been carried out an attempt to discover the mechanisms to improve the therapies and the prognosis of these patients. Some of these studies give the hypothesis that the gastrointestinal tract, more precisely the intestine, can collaborate with metabolome. Extra-intracardiac shunt and HF lead to hypoperfusion and cyanotic heart disease leads to hypoxia. These two conditions make the gastrointestinal tract of these patients to become more mal-absorption to food. Consequently, the poor intestinal microcirculation and resultant dysbiosis may contribute to poor body weight gain and the worsening of prognosis. As known, probiotics can help to maintain or recover the microbiota and maintain a healthy intestinal barrier. In view of the importance of microbiota to the metabolism and the possible beneficial effect in the prognosis of heart-failure patients and the performance of microbiota in maintenance of intestinal barrier, this study has as primary objective to verify the influence of supplementation of the probiotic Lactobacillus Rhamnosus in the patients with CHD.

Malabsorption and dysbiosis in patients with CHD Poor body weight gain and failure to thrive is a very common condition in patients with congenital heart disease (CHD). Dysbiosis occurs in patients with CHD. Such dysbiosis and intestinal barrier dysfunction may become worsen after they underwent cardiopulmonary bypass, and complicate the prognosis of CHD.

Probiotics and Metabolome in Heart failure Cumulative evidence shows increasing importance of microbiota and cardiovascular disease and health. Metabolomic changes are found in CHD patients with hypoxia. It is suggested that Lactobacillus strains function to promote cardiovascular-related conditions. However, the effect of probiotic administration on CHD remains controversial. The investigators propose that hypothesis that Lactobacillus Rhamnosus directly improve the body weight gain and indirectly improve the outcome of patients with CHD. Accordingly, the investigators initiate this clinical trial to testify the beneficial effect of Lactobacillus Rhamnosus on CHD.

Eligibility

Sex
ALL
Min age
1 Month
Max age
3 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients at ages ≤ 3 years old with congenital structure/valvular heart disease and cardiomyopathy with varying degrees of HF NYHA/ROSS functional class and ejection fraction ≥ 35% by echocardiography at the entry of study; 2. No recent 1-month hospitalizations for HF decompensated; 3. Have signed the Free and Informed Consent Form. Exclusion Criteria: 1. CHD with NYHA functional class IV or ejection fraction \< 35%; 2. Do not accept to participate in the study or do not sign the Free and Informed Consent Form; 3. Have used antibiotics and/or corticosteroids and/or other formula containing probiotics in the last 30 days prior enrollment; 4. Clinical conditions that can affect the inflammatory profile such as inflammatory bowel disease, arthrosis, among others; 5. Chronic severe diarrhea (\> 2 weeks; \> 5 times/day) in the last 3 months; 6. Have been submitted to a cardiac surgery or other surgery in the last 3 months; 7. Severe lactose intolerance; 8. Profound anemia (WBC\> 15000, Hb\< 8 ) or hematologic disorder, severe hepatic dysfunction (GPT\> 100), renal function (Cr\> 1.5), abnormal stool analysis or active infection status (CRP\> 10).

Primary outcome measure(s)

  • Percentile of body weight gain — From enrollment to the end of treatment an average of 24 weeks.
    The difference of body weight percentile from the enrollment as the base line to the end of 24-wk treatment (Body weight percentile will be calculated according to the Taiwan children growth reference:https://growth.healthinfo.tw )

Trial sites (1)

FacilityCityRegionStatus
Kaohsiung Chang Gung Memorial Hospital and Chang Gung University Kaohsiung City Taiwan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06872320 on ClinicalTrials.gov ↗ ← All trials in Taiwan