The efficacy of Bifidobacterium quadruple viable tablet in the treatment of diarrhea predominant irritable bowel syndrome: protocol for a randomized, double-blind, placebo-controlled, multicenter trial

Trials. 2020 Jun 30;21(1):597. doi: 10.1186/s13063-020-04490-0.

Abstract

Background: Irritable bowel syndrome (IBS) is one of the most common functional gastrointestinal disorders characterized by recurrent abdominal pain associated with defecation or a change in bowel habits. Leading to significant negative effect on patients' quality of life and huge financial burden to health system, the management of IBS is a great challenge. Probiotics are considered as an effective therapy; however, in a lack of high-quality evidence of efficacy, no strain- and dose-specific probiotics were recommended in clinical guidelines. This study aims to evaluate the efficacy of the Bifidobacterium quadruple viable tablet in the treatment of IBS-D.

Methods/design: A multicenter randomized controlled trial will be performed in fourteen hospitals. A total of three hundred patients who fulfill the eligibility criteria will be stratified divided into an experimental group and a control group randomly in a ratio of 1:1. The experimental group is treated with the Bifidobacterium quadruple viable tablet while the control group is treated with placebo. All the patients will receive a 4-week treatment and a 2-week follow-up. The primary outcome is the effectiveness in improving abdominal pain and stool consistency; the secondary outcome includes evaluation of overall symptom relief, frequency of defecation, bloating, urgency of defecation, remedial medication, score of IBS-QOL, and changes of microbiota and metabonomics. Physical examination, vital signs, laboratory tests, adverse events, and concomitant medication will be taken into account for intervention safety assessment during the trial.

Discussion: This multicenter randomized controlled trial may provide high-quality evidence on the efficacy of the Bifidobacterium quadruple viable tablet for IBS-D on both physical and mental dimensions in China. To fill the gap of previous probiotic intervention studies, in addition, this study will also present safety assessment which will be a significant emphasis.

Trial registration: ChiCTR1800017721 . Registered on 10 August 2018.

Keywords: Diarrhea predominant IBS; Efficacy; Irritable bowel syndrome; Probiotics; Randomized controlled trial.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Bifidobacterium
  • China
  • Diarrhea / etiology
  • Diarrhea / microbiology*
  • Diarrhea / therapy*
  • Double-Blind Method
  • Feces / microbiology
  • Humans
  • Irritable Bowel Syndrome / complications
  • Irritable Bowel Syndrome / microbiology*
  • Irritable Bowel Syndrome / therapy*
  • Multicenter Studies as Topic
  • Probiotics / administration & dosage*
  • Quality of Life
  • Randomized Controlled Trials as Topic
  • Severity of Illness Index
  • Tablets
  • Treatment Outcome

Substances

  • Tablets