Postlaparoscopic reduction of pain by combining intraperitoneal normal saline and the pulmonary recruitment maneuver
Completed
- Conditions
- Postlaparoscopic shoulderpain.10029903
- Registration Number
- NL-OMON42258
- Lead Sponsor
- Maxima Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 127
Inclusion Criteria
Women between 18-65 years of age, ASA classification I-II, who are planned for an elective laparoscopic procedure with a benign gynecologic indication.
Exclusion Criteria
-Women who do not speak Dutch
-Women younger than 18 years
-Women who had a midline laparotomy before
-Pregnant women
-COPD/Emphysema
-Daily use of pain medication
-Allergic/intolerance to NSAID*s
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcomes are the incidence and intensity of postlaparoscopic pain<br /><br>in shoulder and upper abdomen at 8, 24 and 48 hours after surgery, using the<br /><br>Visual Analog Score scale (VAS scale). </p><br>
- Secondary Outcome Measures
Name Time Method <p>The secondary outcomes are postoperative use of pain medication, nausea and<br /><br>vomiting, and pulmonary problems. </p><br>