2D vs. 3D Imaging in laparoscopic surgery

Not Applicable

• Conditions: K35.8; K80.20; Acute appendicitis, other and unspecified

• Registration Number: DRKS00005685
• Lead Sponsor: Asklepios Klinik Langen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-02-05
• Study Completion: 2015-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 79

Inclusion Criteria

Patients with informed consent and where the indication for a laparoscopic procedure is given

Exclusion Criteria

Patient with dissent or unable to consent

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Comfort to the surgeon controlled by likert scale / visuell analog scale and raw NASA TLX questionnaire directly after the operation; <br>duration of operation in minutes<br>

Secondary Outcome Measures

Name	Time	Method
adverse events, registered with the clavien dindo classification