跳至主要内容
临床试验/CTRI/2018/05/014021
CTRI/2018/05/014021已完成3 期

A randomised study to evaluate the acute toxicity in patients of locally advanced cervical cancer treated with 3DCRT versus IG-VMAT

POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Previously untreated, biopsy proven squamous cell carcinoma cervix
  • 2. Karnofsky performance scale > 70
  • 3. Pre treatment parameters: -
  • a) HB > 10gm/dl
  • b) Age <= 70 years
  • c) TLC > 4000/cu mm
  • d) Platelets > 1 lakh/cu mm
  • e) Serum urea < 40 mg/dl
  • f) Serum creatinine < 1.2mg/dl
  • g) Normal Chest X-ray
  • 4. Patientâ??s willingness to give informed
  • consent and agree to

排除标准

  • 1. All post operative cases
  • 2. Medical contraindication for concurrent
  • chemotherapy
  • 3. Patients with history of previous
  • malignancies
  • 4. Patients having any uncontrolled co-morbid
  • conditions.

研究者

发起方
POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH

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