A Safety and Efficacy Study of Daikenchuto (TU-100) to Relieve Abdominal Bloating in Female Subjects With Irritable Bowel Syndrome

PHASE2CompletedINTERVENTIONAL
Enrollment

101

Participants

Timeline

Start Date

July 31, 2014

Primary Completion Date

April 30, 2016

Study Completion Date

April 30, 2016

Conditions
Irritable Bowel Syndrome in Females
Interventions
DRUG

TU-100

15g daily, orally as 5g three times daily for 4 consecutive weeks

DRUG

Placebo

Matching placebo given 5g three times daily orally for 4 consecutive weeks

Trial Locations (1)

90095

Oppenheimer Family Center for Neurobiology of Stress Division of Digestive Diseases David Geffen School of Medicine at UCLA, Los Angeles

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ICON Clinical Research

INDUSTRY

lead

Tsumura USA

INDUSTRY