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Effect of Probiotic consumption in individuals with Heart Diseases

Effect of Probiotic supplementation in individuals with Cardiovascular Diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6ztyb7
Enrollment
Unknown
Registered
2020-02-20
Start date
2021-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Myocardial Infarction

Interventions

Randomized, placebo-controlled, triple-blind clinical trial to be conducted at the Hospital Evangélico Sr. e Sra. Goldsby King, Dourados, MS. The study sample will consist of adults and elderly indivi
M1 - intermediate moment, 30 days after supplementation
M2 - final moment, 90 days after supplementation. The supplements and placebo will be pre-packaged in opaque sachets/bottles and sealed by the supplier and coded only with random numbers corresponding
G07.203.300.456.500
G07.203.300.456

Sponsors

Faculdade de Ciências da Saúde da Universidade Federal da Grande Dourados
Lead Sponsor
Universidade Federal da Grande Dourados - UFGD
Collaborator

Eligibility

Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Volunteers aged 20 or over; both sexes; undergoing Myocardial Revascularization for Atherothrombotic Coronary Artery Disease

Exclusion criteria

Exclusion criteria: Previous gastrointestinal diseases; Chronic kidney disease on dialysis; food intolerances or food allergies; alcohol or illicit drug addiction; current or previous use (up to three months) of antibiotics, laxatives and appetite suppressants; regular use of antispasmodics or antacids; current or previous use (up to three months) of dietary fiber modules, prebiotics, probiotics, synbiotics or products enriched with these ingredients; present intolerance to prebiotics, probiotics, synbiotics; pregnant or lactating women; current follow up of unusual diets (vegetarian, paleolithic, gluten free, lactose free, macrobiotic); indigenous people

Design outcomes

Primary

MeasureTime frame
Reduction in C-reactive protein concentrations, verified by laboratory determination of this marker in blood plasma before (baseline) and after 90 days of supplementation (final). The average C-reactive protein concentrations in the intervention group will be compared with the control group

Secondary

MeasureTime frame
Biochemical tests related to lipid profile and glycemic homeostasis (total cholesterol, LDL-c, HDL-c, triglycerides, fasting blood glucose), inflammation (C-reactive protein, cytokines, lipopolysaccharides), anthropometric indicators (adductor pollicis muscle thickness, body mass index, skinfolds, body circumferences and related indices), muscle stregth, gastrointestinal symptoms, and symptoms of depression and anxiety

Countries

Brazil

Contacts

Public ContactRicardo Fernandes

Universidade Federal da Grande Dourados - UFGD

ricardofernandes@ufgd.edu.br+55 (67) 3410-2320

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 12, 2026