The effect of oral administration of a multispecies probiotic product in healthy volunteers and ileostomy patients; double-blind, placebo-controlled, cross-over trial

Completed

• Conditions: Healthy volunteers and ileostomy patients after ulcerative colitis; Digestive System; Ulcerative colitis

• Registration Number: ISRCTN45167712
• Lead Sponsor: Individual Sponsor (Netherlands)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2005-09-12
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

10 healthy volunteers and 10 ileostomy patients after ulcerative colitis

Exclusion Criteria

Use of antibiotics and/or probiotics within 2 weeks prior to randomisation

Study & Design

• Study Type: Interventional
• Study Design: Not specified