CTRI/2025/09/095262招募中3 期
Comparison of toxicities and locoregional control between two high dose rate intracavitary brachytherapy regimens in the patients receiving curative treatment for carcinoma cervix: A Randomised controlled trial
Dept of Radiotherapy1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2025年9月30日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 102
- 试验地点
- 1
- 主要终点
- to compare acute as well as late bowel and bladder toxicities between the 2 regimens.
研究概览
简要总结
The objective of the study is to see if it is feasible to reduce the duration of curative treatment for carcinoma cervix without increasing the acute and late toxicity by adapting the newer regimen.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)（—）
- 性别
- Female
入选标准
- •KPS a more than 70 Stage IB2 to IVA Baseline blood investigation are within normal limit.
- •No previous treatment for the same.
排除标准
- 未提供
结局指标
主要结局
to compare acute as well as late bowel and bladder toxicities between the 2 regimens.
时间窗: At first follow up which is at 8 weeks
次要结局
- To compare loco regional control between the two regimens(At first follow up at 8 weeks, at second follow up at 16 weeks & at third follow up at 24 weeks)
研究者
Dr Ankita Prusty
IGMC SHIMLA
研究点 (1)
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