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RECRUITING
NCT06612411
EARLY_PHASE1

B.Subtilis Attenuate Symptoms in Diarrhea-predominant Irritable Bowel Syndrome by Increasing Hypoxanthine Biosynthesis

Sponsor: Jinling Hospital, China

View on ClinicalTrials.gov

Summary

This is a prospective, single-blind, randomized parallel study to investigate whether B. subtilis could improve clinical symptoms of IBS-D patients. Patients are randomly assigned by envelope method. A senior gastroenterologist is responsible for prescribing medication. Researchers are blind to patients' medication. Participants with IBS are recruited and randomized to receive a 4-week administration of B. subtilis-based probiotics. Clinical symptoms and stool samples are collected before and after the trial.

Official title: Purine Starvation Driven by Host-microbiota Maladaptation Contributes to the Pathogenesis of Irritable Bowel Syndrome

Key Details

Gender

All

Age Range

16 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

180

Start Date

2024-06-01

Completion Date

2024-12-31

Last Updated

2024-09-25

Healthy Volunteers

Yes

Interventions

DRUG

B. subtilis

2 capsules, 3 times a day, orally taken for one month

DRUG

Dead B. subtilis

2 capsules, 3 times a day, orally taken for one month

Locations (2)

Jinling Hospital

Nanjing, China

Jinling Hospital

Nanjing, China