drugset / Trial / NCT00529269

Measurement of Patient Reported Outcomes in Korean Renal Transplant Patients With and Without Gastrointestinal (GI) Symptoms

NCT00529269

Phase 4 Completed 200 enrolled Novartis Pharmaceuticals
Non-randomizedCrossoverSingle-blindTreatment

Summary

This study will evaluate the impact that GI complaints have on patient-reported outcomes and to determine if there is improvement in patient-reported outcomes when converted from mycophenolate mofetil (MMF) to Enteric-coated mycophenolate sodium (EC-MPS)

Timeline

Start
2006-12
Primary completion
2007-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Mycophenolate Sodium Unknown

Indications

No indication recorded.