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LOTRONEX® in Severe Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D) — RELIANCE  

Irritable Bowel Syndrome Clinical Trial

Official title:
Research Study to Evaluate LOTRONEX® in Severe IBS-D: Analysis of Current Clinical Practice Environment

Clinical Trial Summary

An observational study to evaluate LOTRONEX® in women with severe IBS-D in the current clinical practice setting.

Clinical Trial Description

This observational study will evaluate the effect of Lotronex® as used in the current clinical practice setting on symptom relief, specifically, improvement in bowel habits and IBS pain. Patients planning to initiate commercially available LOTRONEX® therapy will be consented for study participation. Patients will complete study questionnaires related to bowel symptoms, prior therapies, quality of life, productivity loss and treatment outcome. Investigators will also be asked to complete questionnaires related to the patient's disease characteristics, patient progress on study medication and treatment outcome. ;

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01257477
Study type Observational
Source Prometheus Laboratories
Contact
Status Completed
Phase N/A
Start date November 2010
Completion date March 2013
View Details
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