drugset / Trial / NCT00158691

Intravenous Versus Subcutaneous Amifostine in Prevention of Xerostomia After RT for Head and Neck Carcinomas

NCT00158691

RandomizedParallel-groupOpen-labelTreatment

Summary

Prospective randomized study in order to compare intravenous versus subcutaneous administration of amifostine in patients receiving radiotherapy for head and neck cancer. Salivary flow will be evaluated during few years after the treatment by a clinical evaluation, the measure of the weight of saliva and a patient benefit questionnaire cotation.

Timeline

Start
2001-03
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject amifostine Unknown 200 mg/m2 Intravenous
Subject amifostine Unknown 500 mg Intravenous

Indications