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临床试验/NCT07568964
NCT07568964尚未招募不适用

Effect of Probiotics on Atrial Fibrillation Outcome in Patients Undergoing Cardioversion

Ain Shams University1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2026年5月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
56
试验地点
1
主要终点
Atrial Fibrillation Recurrence

研究概览

简要总结

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

详细描述

Assessment of AF recurrence: Early AF recurrence is defined as relapse into AF within 1 week following successful cardioversion and AF recurrence through the study's 12-week follow-up.

Patients and Methods Design: Prospective, randomized, open label, controlled clinical trial

Patients: A total of 56 AF patients undergoing cardioversion will be randomly enrolled into one of 2 arms:

  1. Group 1 (Control group) (n=28): AF patients undergoing cardioversion who will receive the standard of care
  2. Group 2 (Probiotic group) (n = 28): AF patients undergoing cardioversion who will receive the standard of care in addition to probiotics DAILY orally administered (Probiotics 25 billion) after cardioversion for 12 weeks.

Groups (1 & 2) will be subjected to cardioversion on admission according to standard protocols and criteria.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Female or male aged 40 years or above with BMI less than 40
  • Persistent AF patients directly after cardioversion

排除标准

  • History of probiotic supplementation in the previous 6 weeks
  • Autoimmune diseases
  • Ongoing treatment with immunosuppressive therapies
  • Active Infection
  • Pregnant or breast-feeding patients
  • Active participation in another clinical study
  • History of or known allergy or intolerability to the study medications

研究组 & 干预措施

Experimental: Control group

Experimental

28 AF patients undergoing cardioversion who will receive standard of care

干预措施: Anticoagulant Therapy (Drug)

Experimental: Probiotic group

Experimental

28 AF patients undergoing cardioversion who will receive the standard of care in addition to Probiotics 25 billion daily orally, after cardioversion for 12 weeks

干预措施: Anticoagulant Therapy (Drug)

Experimental: Probiotic group

Experimental

28 AF patients undergoing cardioversion who will receive the standard of care in addition to Probiotics 25 billion daily orally, after cardioversion for 12 weeks

干预措施: Probiotics capsules (Drug)

结局指标

主要结局

Atrial Fibrillation Recurrence

时间窗: 7 days

次要结局

  • Atrial Fibrillation Recurrence(12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sarah Mostafa Mostafa Abdelfatah Raesah

Teaching Assistant and Researcher in Clinical Pharmacy Department, Faculty of Pharmacy, Ain Shams University.

Ain Shams University

研究点 (1)

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