The effectiveness of intraperitoneal normal saline infusion and the pulmonary recruitment maneuver to reduce postlaparoscopic shoulder and upper abdominal pain in elective gynecologic surgeries

Phase 2

• Conditions: aparoscopy.; Postprocedural disorders of genitourinary system, not elsewhere classified

• Registration Number: IRCT201402022576N8
• Lead Sponsor: Research deputy of Tehran university of medical sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 280

Inclusion Criteria

The patients selected for screening were all required laparoscopic surgery during the study period. The inclusion criteria were female gender, age 20–65 years old; an American Society of Anesthesiologists physical status classification of I or II, and a willing to undergo laparoscopic surgeries for benign gynecologic lesions, including laparoscopically assisted vaginal hysterectomy, myomectomy, and cystectomy. Patients were excluded from randomization if their disease was malignant, or if they were unwilling to participate.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post operative pain. Timepoint: 2, 4, 6, 12, 24 hours after surgery. Method of measurement: VAS analouge.

Secondary Outcome Measures

Name	Time	Method
ausea. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.;Vomiting. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.;Abdominal distention. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.