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A CLINICAL TRIAL TWO COMPARE TO TREATMENT SCHEDULES OF CONCURRENT CHEMORADIATION IN LOCALLY ADVANCED CANCER OF CERVIX.

Phase 3
Registration Number
CTRI/2010/091/000194
Lead Sponsor
DR.ARAVINDH.S.ANAND
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other (Terminated)
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1. women with biopsy proved uterine cancer, less than or equal to 70 yeras of age, locally advancer uerine cancer, WHO P.S 0-1, Normal CBC, LFT, RFT.

Exclusion Criteria

PRIOR CHEMOTHERAPY OR RADIATION, PARA AORTIC LYPH NODE INVOLVEMENT, DISTANT METASTASIS

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Clinical response&amp; local control of disease, disease free survival.<br>2. Delayed toxicityTimepoint: 3 years may extend to 5 years
Secondary Outcome Measures
NameTimeMethod
ACUTE TOXICITY &amp; TOLERABILITYTimepoint: 1 YEAR
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