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Starting soon Not applicable

Evaluation of Probiotics' Effect on Atrial Fibrillation Recurrence in Patients Undergoing Cardioversion

NCT07568964 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-05-10
Last updated
2026-05-06

Condition(s) studied

Atrial Fibrillation (AF)

Investigational drug(s) / intervention(s)

Anticoagulant TherapyProbiotics capsules

Anticoagulant Therapy: Drug: The standard of care for AF management directly following cardioversion Include anticoagulant therapy for at least 4 weeks, rate control therapy, rhythm control therapy, or both as per clinical and guideline decisions.

Probiotics capsules: Probiotics at a of dose 25 billion / 1 capsule will be orally administered daily for 12 weeks

Study summary

The aim of this clinical study is to evaluate the efficacy and tolerability of probiotics on atrial fibrillation recurrence.

Eligibility

Sex
ALL
Min age
40 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Female or male aged 40 years or above with BMI less than 40 2. Persistent AF patients directly after cardioversion Exclusion Criteria: 1. History of probiotic supplementation in the previous 6 weeks 2. Autoimmune diseases 3. Ongoing treatment with immunosuppressive therapies 4. Active Infection 5. Pregnant or breast-feeding patients 6. Active participation in another clinical study 7. History of or known allergy or intolerability to the study medications

Primary outcome measure(s)

  • Atrial Fibrillation Recurrence — 7 days

Trial sites (1)

FacilityCityRegionStatus
Ain Shams University's Hospital Cairo Egypt

Other trials for the same condition

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 NCT07568964 on ClinicalTrials.gov ↗ ← All trials in Egypt