Case-control study single port cholecystectomy versus conventional cholecystectomy

• Conditions: Complications following laparoscopic cholecystectomy; K80.20

• Registration Number: DRKS00003122
• Lead Sponsor: Asklepios Klinik LangenAkademisches Lehrkrankenhaus Goehte-Universität Frankfurt

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2011-07-01
• Study Start: 2011-09-12
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

chronic and acute cholecystolithiasis

Exclusion Criteria

previous laparotomies, liver cirrhosis

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary endpoint is the postoperative complication rate. The complication rate is evaluated in the postoperative hospital stay.

Secondary Outcome Measures

Name	Time	Method
cosmetic results