Protocol of efficacy of bifidobacteria intake on gastrointestinal symptoms in symptomatic type 2 diabetes mellitus patients in abdominis: An open-label, randomized controlled trial (Binary STAR study)

PLoS One. 2024 Jan 11;19(1):e0295998. doi: 10.1371/journal.pone.0295998. eCollection 2024.

Abstract

Background: This randomized, parallel-group study aims to investigate the effects of the probiotic Bifidobacterium bifidum G9-1 (BBG9-1) on the symptoms of diarrhea or constipation in patients with type 2 diabetes mellitus (T2DM).

Methods: This study will examine 100 patients with T2DM who suffering from symptoms of diarrhea or constipation. Eligible patients will be randomly assigned 1:1 to two groups (group A, BBG9-1 group; group B, control group), after the baseline examination. Patients assigned to group A will receive probiotic BBG9-1 oral administration along with their current treatment for 12 weeks, and patients assigned to group B will continue the current treatment for 12 weeks without probiotic BBG9-1 oral administration. Subsequently, examinations similar to the baseline examinations will be performed. The primary endpoint will be a change in the Gastrointestinal Symptom Rating Scale (GSRS) total score from baseline to week 12. Secondary endpoints will include the following: change and percent change in parameters such as GSRS subdomain scores, fecal properties/Bristol stool form scale, defecation frequency, biomarkers, gut microbiota, and macronutrients and factors that affect GSRS total score or constipation/diarrhea subdomain scores from baseline to week 12.

Discussion: The results of this study will clarify the utility of probiotic BBG9-1 in the treatment of diarrhea or constipation in patients with T2DM.

Trial registration: jRCTs051220127.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Bifidobacterium
  • Bifidobacterium bifidum*
  • Constipation / therapy
  • Diabetes Mellitus, Type 2* / complications
  • Diarrhea / microbiology
  • Double-Blind Method
  • Gastrointestinal Diseases* / complications
  • Humans
  • Probiotics* / pharmacology
  • Probiotics* / therapeutic use
  • Randomized Controlled Trials as Topic
  • Treatment Outcome

Grants and funding

This study was supported by Biofermin Pharmaceutical Co., Ltd. Funding information is also upload at the "Source of Monetary Support / Secondary Sponsor" section in jRCT as the funding is provided by Biofermin Pharmaceuticals (https://jrct.niph.go.jp/en-latest-detail/jRCTs051220127).