Postlaparoscopic reduction of pain by combining intraperitoneal normal saline and the pulmonary recruitment maneuver

Completed

• Conditions: laparoscopy; laparoscopieshoulder pain; schouderpijnintraperitoneal saline; fysiologisch zout intraperitoneaalpulmonary recruitment maneuver

• Registration Number: NL-OMON27538
• Lead Sponsor: Dr. M.Y. Bongers, gynecologist Máxima Medisch Centrum VeldhovenDe Run 4600, 5504 DB Veldhovene-mail: M.Bongers@mmc.nl Phone (office): +31 40 888 8384

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 126

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcomes are the incidence and intensity of postlaparoscopic pain in shoulder and upper abdomen at 8, 24 and 48 hours after surgery, using the Visual Analog Score scale (VAS scale).

Secondary Outcome Measures

Name	Time	Method
The secondary outcomes are postoperative use of pain medication, nausea and vomiting, and pulmonary complications.