Randomized controlled trial on the effect of the residual pneumoperitoneum on postoperative pain after laparoscopic cholecystectomy
Not Applicable
- Conditions
- K80Cholelithiasis
- Registration Number
- DRKS00023286
- Lead Sponsor
- Klinik für Allgemein- und Viszeralchirurgie, Evangelisches Krankenhaus Lippstadt gemeinnützige GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Indication for elective laparoscopic cholecystectomy because of cholelithiasis
Exclusion Criteria
Planned simulatenous operations; emergency surgery; pregnancy; lack of written informed consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome measure is the intensity of pain under strain (e.g. while coughing) on the evening of the day of surgery. Maximum pain intensity will be elicited from the patient using the numerical rating scale (NRS, 0 to 10 scale).
- Secondary Outcome Measures
Name Time Method Duration of surgery; severe adverse events; pain (measured with the numerical rating scale); length of hospital stay