None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Histologically proven squamous cell carcinoma of oral cavity 2.T1 to T4a(skin) N0 N1 disease intended to be treated with radical radiotherapy 3.ECOG Performance Status 0,1 4.Patients willing to participate in the study.
Exclusion criteria
Exclusion criteria: 1.Age 70 yrs. 2.Non squamous cell carcinoma of head and neck region 3.N2 & above 4.Field size > 81 sq cm 5.Prior chemotherapy & radiotherapy 6.Metastatic disease 7.Pregnant women 8.Mentally unfit to give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Response Rate 2.Toxicity 3.QOLTimepoint: 5 TO 6 MONTHS AFTER COMPLETION OF TREATMENT | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Disease free survival 2.Overall survival Timepoint: 5 TO 6 MONTHS AFTER COMPLETION OF TREATMENT | — |
Countries
India
Contacts
REGIONAL CANCER CENTRE TRIVANDRUM