drugset / Trial / NCT00652834

Small Bowel Capsule Endoscopy Findings in Patients Receiving Cellcept®

NCT00652834

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to learn more about symptoms and gastrointestinal lesions associated with taking myfortic® by switching patients to a delayed release formulation that is developed to alleviate GI symptoms. A comparison of the frequency and severity of GI symptoms observed in patients treated with MMF (cellcept®) after conversion to myfortic® will be measured by using a self-assessed questionnaire called Gastrointestinal Symptom Rating Scale (GSRS). To prove the incidence and improvement of GI lesions in patients treated with MMF (cellcept®) after conversion to myfortic® will be measured by using Small Bowel Capsule Endoscopy (SBCE).

Timeline

Start
2009-04
Primary completion
2011-03
Completion
2011-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Mycophenolate Sodium Unknown