Intestinal Microecology in Chronic Constipation

PHASE1CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

April 30, 2010

Primary Completion Date

February 29, 2012

Study Completion Date

February 29, 2012

Conditions
Other ConstipationIrritable Bowel Syndrome
Interventions
DRUG

Lubiprostone

Following the initial stool and breath collections and because of differences in the FDA-approved dosing for the 2 subtypes of chronic constipation, (that is, chronic constipation (CC) versus constipation due to irritable bowel syndrome (C-IBS), the CC subjects received open-label lubiprostone 24 mcg orally twice daily for 4 weeks; while the C-IBS subjects received open-label lubiprostone 8 mcg orally twice daily for 4 weeks.

Trial Locations (1)

85259

Mayo Clinic Arizona, Scottsdale

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Arizona State University

OTHER

collaborator

Takeda Pharmaceuticals North America, Inc.

INDUSTRY

lead

Mayo Clinic

OTHER

NCT00934479 - Intestinal Microecology in Chronic Constipation | Biotech Hunter | Biotech Hunter