drugset / Trial / NCT01066741

Prevention of Radiation-induced Severe Oral Mucositis in Oral Cavity, Oropharynx, Hypopharynx, and Cavum Cancer

NCT01066741

Phase 3 Terminated 78 enrolled Centre Leon Berard BOIRON · collab
RandomizedParallel-groupSingle-blindPrevention

Summary

The purpose of this study is to evaluate the benefit of a mouthwash with a phytopharmaceutical preparation, Homeodent®, compared to a mouthwash solution containing sodium bicarbonate, for prevention of severe mucositis (grade ≥3, RTOG classification) in patients receiving irradiation for oral cavity, oropharynx, hypopharynx or cavum cancer. This is a phase III, controlled, randomized, single blind study. The estimated inclusion period is approximately 24 months. The number of patients required in this monocentric study is 330 (165 per arm).

Timeline

Start
2009-05
Primary completion
2011-02
Completion
2011-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Homeodent® Unknown 5 ml Other
Comparator sodium bicarbonate Diagnostic / imaging agent 125 ml Other