Acute toxicities and dosimetry associated with conventional and hypo fractionated adjuvant radiation in carcinoma breast.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- To evaluate the acute reactions IN both conventional and hypo fractionated regimens.
研究概览
简要总结
The study aims to evaluate the acute reactions and dosimetry in conventional fractionationated radiotherapy compared to hypofractionated radiotherapy in breast cancer patients. It also aims to assess the doses to the organs at risk. The research question or hypothesis is that hypo - fraction radiotherapy is comparable to convntional fractionation radiotherapy in terms of acute adverse effects and dosimetric parameters.Aditionally hypo-fractionated radiotherapyis expected to improve patient compliance.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients who are above the age of 18 years diagnosed with early stage or locally advanced carcinoma breast, has undergone mastectomy or breast conservative surgery who will be required to undergo adjuvant radiotherapy.
排除标准
- •PATIENTS WITH METASTATIC DISEASE PATIENTS WITH RELAPSE MENTALLY CHALLENGED PATIENTS.
结局指标
主要结局
To evaluate the acute reactions IN both conventional and hypo fractionated regimens.
时间窗: BEFORE THE STARTING OF THE TREATMENT 0 WEEK | DURING THE TREATMENT 4 TH WEEK | POST TREATMENT 2 MONTH 6 MONTHS
次要结局
- To assess the quality of life(At the end of the treatment)
研究者
YENEPOYA UNIVERSITY MEDICAL COLLEGE HOSPITAL
DEEMED TO BE UNIVERSITY NABH ACCREDITATED