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
Trial end date:
2018-12-31
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Treatments:
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.