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临床试验/NCT01558414
NCT01558414已完成3 期

Prospective Randomized Clinical Trial Comparing Single Incision Laparoscopic Surgery vs Flexible Single Incision Surgery on Cholecystectomy

Jose F. Noguera2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年4月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Surgical safety

研究概览

简要总结

Prospective randomized pilot clinical trial, with 3 arms and one year follow up. The study will include 60 patients, with a 1:1:1 ratio, 20 patients per group. In 40 patients a transumbilical single site incision will be performed with two different manners: single-port device SILS TM (Single Incision Laparoscopic Surgery), and flexible endoscope and accessory trocars in a single incision (FSIS-Flexible Single Incision Surgery). The third group is the control one, a conventional laparoscopic approach.

The trial is designed as a pilot study to assess, as main objective, if these two endoscopic approaches have the same security and effectiveness in cholecystectomy.

Hypothesis:

Transumbilical approaches with single port and single incision with the flexible endoscope have the same efficacy and safety performing the endoscopic cholecystectomy.

Objectives:

Main objective:

Assess whether both approaches are equally safe in its application to endoscopic cholecystectomy.

Secondary objectives:

Investigate the differences in the rate of conversion to open surgery between different surgical approaches.

Investigate the differences in the rate of wound infection between the different surgical approaches.

Investigate the differences in the rate of postoperative incisional hernias between different surgical approaches.

Investigate whether there are differences in the rate of overall complications, all-cause mortality and the cost between different surgical approaches.

详细描述

Inclusion criteria:

  • Patients affected with symptomatic cholelithiasis with elective surgical indication, not urgent, aged between 18 and 65.
  • Signing of informed consent for cholecystectomy and specific consent for the trial.
  • Anesthetic risk ASA I-II.

Exclusion criteria:

  • Presence of acute cholecystitis and / or suspicion of occupation of the main bile duct.
  • ASA III and higher.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age over 18 and under 65
  • symptomatic cholelithiasis with an indication for laparoscopic surgery
  • signed specific informed consent including specific information of the new surgical approach
  • ASA 1 and 2.

排除标准

  • current or previous cholecystitis
  • current or previous suspected bile duct's problems
  • previous abdominal surgery
  • umbilical and other abdominal hernias
  • some other condition with increased risk to infection or abdominal wall problems.
  • ASA 3 and more

结局指标

主要结局

Surgical safety

时间窗: During surgical intervention

Number of patients without clinical problems in the surgery

次要结局

  • Conversion to other surgical approach(During the surgical intervention)

研究者

发起方
Jose F. Noguera
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jose F. Noguera

Chief Department of Surgery

Hospital Son Llatzer

研究点 (2)

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