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Clinical Trials/NCT01558414
NCT01558414
Completed
Phase 3

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

Jose F. Noguera1 site in 1 country60 target enrollmentApril 2011

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Cholelithiasis
Sponsor
Jose F. Noguera
Enrollment
60
Locations
1
Primary Endpoint
Surgical safety
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
November 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Jose F. Noguera
Responsible Party
Sponsor Investigator
Principal Investigator

Jose F. Noguera

Chief Department of Surgery

Hospital Son Llatzer

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Surgical safety

Time Frame: During surgical intervention

Number of patients without clinical problems in the surgery

Secondary Outcomes

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

Study Sites (1)

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