The Efficacy of Sodium Butyrate and Probiotics in Patients With Irritable Bowel Syndrome

NACompletedINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

April 15, 2021

Primary Completion Date

September 30, 2023

Study Completion Date

January 31, 2024

Conditions
Irritable Bowel Syndrome
Interventions
DIETARY_SUPPLEMENT

Probiotics and microcapsulated sodium butyrate

The patients who give their consent to take part in this study, will receive an oral microencapsulated sodium butyrate and a mixture of probiotics formulation 2 times a day for a period of 12 weeks.

DIETARY_SUPPLEMENT

Maltodextrin

The patients who give their consent to take part in this study will receive an oral maltodextrin as placebo 2 times a day for a period of 12 weeks.

Trial Locations (1)

90-647

Medical University of Lodz, Lodz

All Listed Sponsors
collaborator

Medical University of Lodz

OTHER

lead

Nordic Biotic Sp. z o.o.

INDUSTRY