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Clinical Trials/NCT02357589
NCT02357589
Completed
Not Applicable

3 Versus 2 Dimensional HD Laparoscopy in Cholecystectomy: a Prospective, Single Blinded, Randomized, Controlled Trial

Helsinki University Central Hospital1 site in 1 country210 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cholecystolithiasis
Sponsor
Helsinki University Central Hospital
Enrollment
210
Locations
1
Primary Endpoint
Duration of surgery
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The 3D-systems have emerged also to the world of surgery, and the three-dimensional laparoscopic systems are gradually entering the operating rooms. In the normal laparoscopy there are only two-dimensional view, which is somewhat challenging when operating in three-dimensional environment. Even though the 3D-systems have been widely studied in laboratory circumstances, there are still no evidence of benefits of 3D vs 2D in clinical point of view and no prospective randomized trials have been published. Therefore, the purpose of this study is to investigate is there something to gain in changing into 3D laparoscopic system for cholecystectomy (LCC).

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
May 10, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hanna Koppatz

MD

Helsinki University Central Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for laparoscopic cholecystectomy

Exclusion Criteria

  • Some other surgical operation planned during LCC
  • Expected major risk of conversion (e.g. multiple previous abdominal operation, previous peritonitis, previous cholecystitis)
  • Operating surgeon experience less than 5 3D laparoscopy operations

Outcomes

Primary Outcomes

Duration of surgery

Time Frame: Expected average time of surgery 1 hour

Secondary Outcomes

  • Intraoperative complications(During the operation, expected average time of surgery 1 hour)
  • Complications, Clavien-Dindo classification(30 days after randomization)
  • Postoperative stay in hospital(Expected range 0-7 day)
  • Bleeding(During the operation, expected average time of surgery 1 hour)
  • Mortality(30 days after randomization)
  • Need for conversion into open surgery(During the operation, expected average time of surgery 1 hour)
  • Total need of opioids in milligrams(Expected range 0-7 day)
  • Operation theatre time(Expected average 1,5 hours)
  • Number of participants with readmission(s)(30 days after randomization)
  • Postoperative pain, VAS(Expected range 0-7 day)

Study Sites (1)

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