CTRI/2023/04/051952
Not yet recruiting
未知
A Prospective Randomised Study To Evaluate Efficacy And Safety between Two Different Dose Fractionation Schedule Of Interstitial Brachytherapy In Treatment Of Patients With Carcinoma of Uterine Cervix
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: C531- Malignant neoplasm of exocervix
- Sponsor
- SVIMS
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Histopathologically confirmed carcinoma of Uterine cervix
- •Patients of age group 18 to 70 years.
- •Patients with performance status of 0 to 2
- •Stage II B\- III C with intact cervix.
- •Patients with gross residual disease after EBRT not suitable for ICRT
- •Distorted Geometry like narrow vagina and os not soundable
- •Post hysterectomy Carcinoma vault
- •Post supra cervical hysterectomy with carcinoma of cervical stump.
- •Extensive para vaginal and distal vaginal involvement
- •Patients who has given approved informed consent
Exclusion Criteria
- •Patients with distant metastasis
- •Patients with prior EBRT and Brachytherapy to pelvis
- •Patients with ECOG performance status of 3\-4
- •Pregnant women and lactating mothers
- •Patients who has not given informed consent
Outcomes
Primary Outcomes
Not specified
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