Overview
Prospective Study of Head and Neck Cancer Radiation Treatment With or Without Amifostine
Status:
Suspended
Suspended
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to compare the incidence of stomatitis when treating with amifostine before radiation treatment.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Sun Pharmaceutical Industries LimitedTreatments:
Amifostine
Criteria
Inclusion Criteria:1. 18-70 years old, male or female
2. Primary treatment of phase I-IVA head and neck cancer patients, identified by
histological and pathological diagnosis
3. Postoperative patients should receive radiation treatment in 12 weeks
4. ECOG <2
5. Expected lifetime ≥6months
6. No severe complications (hypertension, CHD, diabetes and psychiatric history, etc.)
7. Not involved in other clinical trials
8. Sign ICF
Exclusion Criteria:
1. ECOG >2
2. Suffered other cancers in the past 5 years
3. Received amifostine treatment in the past 4 weeks
4. Unable to complete treatment or sign ICF because of medical or physical reasons