Overview
An Experimental Study to Compare Treatment Response and Toxicities of Concurrent Chemoradiation With Weekly Cisplatin and Three Weekly Cisplatin in Locally Advanced Head and Neck Cancer.
Status:
Completed
Completed
Trial end date:
2018-12-31
2018-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of this study is to compare treatment responses and toxicities of concurrent chemo-radiation with weekly and three weekly Cisplatin in locally advanced Head & Neck Cancer. Half of the participants received Cisplatin (40 mg/m2) weekly with radiotherapy, while the other half received Cisplatin (100 mg/m2) thrice weekly with radiotherapy. Radiotherapy continued five days per week for six and half weeks.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Bangabandhu Sheikh Mujib Medical University, Dhaka, BangladeshTreatments:
Cisplatin
Criteria
Inclusion Criteria:- Biopsy proved, previously untreated, Squamous cell carcinoma of head & neck
- Stages III to IVB
Exclusion Criteria:
- Patients with history of prior chemotherapy or radiotherapy to the head and neck
region.
- Initial surgery (excluding diagnostic biopsy) of the primary site.
- Patients with synchronous primaries.
- Those who are not willing to be included in the study.
- Pregnant or lactating woman.
- Serious medical illness
- Prisoners.