Study to Evaluate the Treatment Benefits of Probiotic Clostridium Butyricum CBM588® for IBS-D

NACompletedINTERVENTIONAL
Enrollment

405

Participants

Timeline

Start Date

November 10, 2024

Primary Completion Date

February 24, 2025

Study Completion Date

March 10, 2025

Conditions
IBS-D (Diarrhea-predominant)
Interventions
DIETARY_SUPPLEMENT

Probiotic Clostridium butyricum CBM588®

This group received probiotic Clostridium butyricum CBM588® treatment for IBS-D as three tablets daily for 8 weeks.

OTHER

Standard of care IBS-D treatment

Patients in this group received standard of care IBS-D treatment of Trimebutine maleate maleate and followed a lactose-free, no-slag diet.

Trial Locations (1)

Unknown

Quisisana Clinic, Itala

All Listed Sponsors
collaborator

"University of Urbino Carlo Bo"

OTHER

lead

Liaquat University of Medical & Health Sciences

OTHER

NCT06676514 - Study to Evaluate the Treatment Benefits of Probiotic Clostridium Butyricum CBM588® for IBS-D | Biotech Hunter | Biotech Hunter