drugset / Trial / NCT00172367

Chemoprevention Trial for Uremia-Associated Urothelial Carcinoma

NCT00172367

Phase 2 Withdrawn 80 enrolled National Taiwan University Hospital
Non-randomizedParallel-groupOpen-labelPrevention

Summary

Primary Objective: To study if lycopene can improve the biomarker status of urothelial cells in patients with uremia-associated urothelial carcinoma. Secondary Objective: To evaluate the general safety and tolerability of oral lycopene 30 mg per day for 12 weeks in uremic patients.

Timeline

Start
2006-01
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Lycopene Other / unclassified 30 mg Oral