A clinical trial to assess the efficacy of using a rectal bladder spacer balloon for treatment of cancer cervix
Phase 2
Completed
- Conditions
- Health Condition 1: null- Carcinoma Cervix
- Registration Number
- CTRI/2009/091/000840
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Carcinoma Cervix
Suitable for HDR intracavitary brachytherapy
Stage Ib -IIIB
Treated with radical radiotherapy
Exclusion Criteria
Allergy to Latex Balloon
Stage IIIA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method