跳至主要内容
临床试验/CTRI/2018/08/015338
CTRI/2018/08/015338已完成不适用

A Non-interventional, multicentre study to assess prevalence of BRCA1 and BRCA2 mutation among ovarian, primary peritoneal and fallopian tube cancer patients in India ( BRCA Study)

AstraZeneca Pharma India Ltd1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2018年1月10日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
240
试验地点
1
主要终点
The proportion of previously and newly diagnosed ovarian, primary peritoneal or fallopian tube cancer patients with BRCA1 or BRCA2 mutations positive status.

研究概览

简要总结

This is a non-interventional, cross-sectional, multicentre, prospective, observational study to be conducted at 15 sites from different geographical regions across India. The study targets to enrol 240 patients with nearly 16 patients per site over 6 months. The study will enrol females with diagnosis of ovarian, primary peritoneal, or fallopian tube cancer. No study medication will be prescribed or administered as a part of study procedure.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
Female

入选标准

  • Patients who provide written informed consent
  • Female ≥ 18 years of age
  • Previously or newly diagnosed ovarian, primary peritoneal, or fallopian tube cancer patients.

排除标准

  • Patient with any medical condition that, in the opinion of the investigator, would interfere with safe completion of the study
  • Patient participating in any other clinical study/ trial.

结局指标

主要结局

The proportion of previously and newly diagnosed ovarian, primary peritoneal or fallopian tube cancer patients with BRCA1 or BRCA2 mutations positive status.

时间窗: One day

次要结局

  • 1. Level of association between histopathological type and BRCA 1/BRCA 2 mutation positive status(One day)
  • 2. To assess the association of BRCA1/BRCA2 mutation positive status and family history of breast and/or ovarian cancer and any cancer.(• Patients having Family history of Ovarian cancer in first degree relative)
  • 3. To determine the BRCA1/BRCA2 mutation distribution in Indian population.(NA)

研究者

申办方类型
Pharmaceutical industry-Global

研究点 (1)

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