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临床试验/NCT03624764
NCT03624764已完成不适用

A Randomized Comparative Study of Assisted Promontofixation Using Glue Versus Promontofixation Using Threads

Clinique Beau Soleil1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2017年1月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
Operative time

研究概览

简要总结

The treatment of gynecological prolapse (organ removal) can be done by laparoscopy or vaginally. Laparoscopy is used in 1 out of 2 cases, but learning is difficult and operation time is long. One of the technical difficulties is related to the sutures to the threads. Some surgeons therefore use a glue to fix prosthetic reinforcements more easily and quickly, but this sizing technique has only been evaluated very little. Our study proposes to compare the technique of suture with the thread at the gluing of the prostheses in order to validate the merits of this new technique

详细描述

Laparoscopic promontofixation is a surgical technique considered by some as the reference technique. Its difficulty of learning and the duration of operation are factors limiting its diffusion. The use of cyanoacrylate glue is proposed to simplify the procedure, without there being any comparative studies between the sutures over and the sizing of prosthetic reinforcements.

The main objective of the study is to compare the operative time of promontofixation by coelioscopy with suture using threads to promontofixation using glue.

Secondary objectives are the comparison between the two groups of complications per and postoperative, objective anatomical results and functional results of the tissue reaction judged by clinical examination (palpation) and ultrasound and direct cost.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Age> 40 years
  • •Surgical indication of prolapse cure by promontofixation
  • •Valid social insurance
  • •French spoken and written
  • •Informed consent signed

排除标准

  • •Exclusion Criteria:
  • •Concomitant rectopexy
  • •Concomitant Hysterectomy
  • •Associated surgical procedure not compatible with measurement of operative time
  • •Refusal to participate in the study
  • •Pregnant or lactating woman (Article L 1121-5 of the french code of public health)
  • •Vulnerable persons (Article L 1121-6 of the french code of public health)
  • •Majors subject to legal protection or unable to express their consent (Article 1121-8 of the CSP)
  • •Participation in another protocol for less than 3 months
  • •Patient does not have all the inclusion criteria.

研究组 & 干预措施

Promontofixation using glue

Experimental

Patients in this arm will have a laparoscopic promontofixation using a biocompatible cyanoacrylate adhesive replacing some sutures to maintain the strips.

干预措施: Laparostopic promontofixation using surgical glue (Procedure)

Promontofixation using threads

Active Comparator

Patients in this arm will have a laparoscopic promontofixation using sutures with threads to maintain the strips.

干预措施: Laparostopic promontofixation using threads (Procedure)

结局指标

主要结局

Operative time

时间窗: one day

The time elapsed between incision and closure

次要结局

  • Collection of complications at 6 weeks(6 weeks)
  • Collection of intra-operative complications(one day)
  • Collection of per-operative complications(one day)
  • Tolerance of the prosthesis(12 months)
  • Objective anatomical results at 6 weeks(Before surgery)
  • Objective anatomical results at 6 months(6 months after surgery)
  • Objective anatomical results at 12 month(12 months after surgery)
  • Quality of life: pelvic floor distress(12 months after the surgery)
  • Tolerance of the prosthesis(6 weeks)
  • Tolerance of the prosthesis(6 months)
  • Quality of life: pelvic floor distress(Before the surgery)
  • Quality of life: pelvic floor distress(6 months after the surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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