跳至主要内容
临床试验/NCT01851746
NCT01851746Unknown不适用

A Study of Docetaxel and Lobaplatin vs. Docetaxel and Carboplatin Combination Regimen in Patients With Platinum-sensitive (>6 Months) Relapsed Ovarian Cancer

Wuhan University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
200
试验地点
1
主要终点
Evidence of the effectiveness and security of lobaplatin combined with docetaxel in treatment of the sensitive recurrent ovarian cancer.

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness and security of lobaplatin combined with docetaxel in treatment of the sensitive recurrent ovarian cancer.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • age between 18 and 70 years old
  • singed the information consent form
  • Expected survival time >3 months
  • Recurrence for at least 6 months after receiving initial platinum-based chemotherapy and without cytoreductive surgery indications.

排除标准

  • Recurrence within 6 months after receiving initial platinum-based chemotherapy
  • without radiographic evidence for tumor recurrence
  • receiving other chemotherapy, hormone therapy, immunotherapy, or radiation therapy

结局指标

主要结局

Evidence of the effectiveness and security of lobaplatin combined with docetaxel in treatment of the sensitive recurrent ovarian cancer.

时间窗: from pre-chemotherapy to 4-6 weeks post-chemotherapy

Blood routine, urine routine, hepatic and kidney function, electrolyte, ECG, CT,MRI

次要结局

未报告次要终点

研究者

发起方
Wuhan University
申办方类型
Other
责任方
Principal Investigator
主要研究者

HB Cai

Director of gynecologic oncology department of Zhongnan Hospital of Wuhan University

Wuhan University

研究点 (1)

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