Viewing Study NCT06612411



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06612411
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-12

Brief Title: BSubtilis Attenuate Symptoms in Diarrhea-predominant Irritable Bowel Syndrome by Increasing Hypoxanthine Biosynthesis
Sponsor: None
Organization: None

Study Overview

Official Title: Purine Starvation Driven by Host-microbiota Maladaptation Contributes to the Pathogenesis of Irritable Bowel Syndrome
Status: RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None