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3D HD Versus 2D HD in Laparoscopic Inguinal Hernia Repair: a Randomized Controlled Trial

NCT02396940 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-03-02

No results posted yet for this study

Summary

The aim of this study is to compare 3D-laparoscopy versus 2D-laparoscopy with the use of HD resolution in inguinal hernia repair in terms of error rating, performance time and subjective assessment.

Conditions

  • Hernia, Inguinal
  • Hernia

Interventions

DEVICE

3D HD laparoscopy

Olympus 3D laparoscopy ENDOEYE FLEX in high definition with the use of passive, polarizing glasses.

DEVICE

2D HD laparoscopy

Placebo

Sponsors & Collaborators

  • Herlev Hospital

    lead OTHER

Principal Investigators

  • Charlotte Fergo · Herlev Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02396940 on ClinicalTrials.gov