The effect of low pressure pneumoperitoneum and pulmonary recruitment maneuver on postoperative pain after laparoscopic cholecystectomy
Completed
- Conditions
- Optimalisation of pain relief after laparoscopic cholecystectomySurgeryLaparoscopic cholecystectomy
- Registration Number
- ISRCTN17470334
- Lead Sponsor
- AZ Groeninge Dienst Anesthesie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
1. Patients for elective laparoscopic surgery for gall stone disease
2. ASA I and II
3. More than 18 years old
Exclusion Criteria
1. Refusal to give consent
2. Cholecystitis
3. BMI above 35
4. Intolerance to one of the pain medication
5. Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain relief during the first 24 hours is measured using the VAS (visual analogue scale) at fixed time point: 0-1-6-12-18-24 hours postoperatively.
- Secondary Outcome Measures
Name Time Method 1. Total analgesic use during the first 24 hours is measured: the amount of using/needing painkilling during hospitalisation (difference in need of morphine sulphate and tramadol IV (in milligram))<br>2. Recovery after 48 hours is measured using the postoperative 15-item patient-rated quality of recovery questionnaire by telephone call<br>3. Nausea and vomiting is measured using patient personal experience<br>4. Length of hospital stay is measured using time in hours<br>5. Requirement for increased pressure during surgery is measured using: the place in the abdomen that is required to operated