drugset / Trial / NCT00172367
Chemoprevention Trial for Uremia-Associated Urothelial Carcinoma
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lycopene | Other / unclassified | 30 mg | Oral |