跳至主要内容
临床试验/NCT04457882
NCT04457882尚未招募不适用

Evaluation of the Safety of Intraperitoneal Laparoscopic Radical Prostatectomy With or Without Drainage Tube: a Singlecentre, Randomised Controlled, and Non-inferiority Study

Shanghai East Hospital1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2023年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
112
试验地点
1
主要终点
The rate of adverse event

研究概览

简要总结

This is a randomized controlled and non-inferiority trial in comparison of intraperitoneal laparoscopic radical prostatectomy without drainage tube between intraperitoneal laparoscopic radical prostatectomy with drainage tube in the safety in men with a localized prostate cancer.

详细描述

This trial is a prospective, single-centre, randomized controlled, and non-inferiority study in which all men with localized prostate cancer. This study aims to determine whether intraperitoneal laparoscopic radical prostatectomy without drainage tube is non-inferior to intraperitoneal laparoscopic radical prostatectomy with drainage tube in the safety in men with a localized prostate cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • age: more than 18 years old, less than 85 years old;
  • Patient who pathologically diagnosed with prostate cancer and plan to undergo radical laparoscopic surgery for prostate cancer;
  • fully understand the clinical trial protocol and sign the informed consent;

排除标准

  • patients with surgical contraindications who cannot accept surgery;
  • patients with non-laparoscopic radical resection of prostate cancer;
  • patients with previous pelvic radiation therapy and complicated abdominal surgery;
  • patients judged by the investigator to be unsuitable to participate in the clinical trial;

结局指标

主要结局

The rate of adverse event

时间窗: 3 month

Any adverse event according to the Clavien-Dindo classification will be recorded

次要结局

  • Intestinal function recovery(3 Months)
  • Hemoglobin(3 Months)
  • Abdominal effusion and cyst(3 Months)
  • Physical recovery(3 Months)

研究者

发起方
Shanghai East Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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