21
Participants
Start Date
April 30, 2010
Primary Completion Date
February 29, 2012
Study Completion Date
February 29, 2012
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.
Mayo Clinic Arizona, Scottsdale
Lead Sponsor
Arizona State University
OTHER
Takeda Pharmaceuticals North America, Inc.
INDUSTRY
Mayo Clinic
OTHER