Skip to main content
Clinical Trials/NCT02004470
NCT02004470UnknownNot Applicable

Lavage and Suction of the Right Upper Quadrant to Reduce Post Laparoscopic Shoulder Pain: A Randomized Controlled Trial

University of Tennessee8 sites in 1 country100 target enrollmentStarted: January 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Locations
8
Primary Endpoint
Pain Score

Study Overview

Brief Summary

The use of laparoscopy in gynecologic surgery has been well established to decrease morbidity, blood loss, hospital stay, and post-operative pain when compared to traditional open abdominal surgery. However, the laparoscopic technique is associated with post-operative shoulder pain.

We hypothesize that a combination of intraperitoneal saline lavage and active suction removal of carbon dioxide gas from the right upper quadrant of the abdomen will decrease incidence of post-laparoscopic shoulder pain when compared to passive exsufflation of carbon dioxide gas.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • English speaking patient
  • Age 18-75
  • must undergo laparoscopic surgery
  • willing to participate in the study

Exclusion Criteria

  • Male patients
  • Under 18 or older than 75
  • Laparoscopic procedures that get converted to laparotomy
  • Intraoperative hemorrhage more than 500 cc
  • Patients with active joint disease
  • History of shoulder surgery
  • Intraoperative laceration to the liver
  • Malignancy
  • Long term daily narcotic use
  • Chronic right upper quadrant/ shoulder pain
  • Pregnancy
  • History of dementia, Alzheimers, stroke or other condition causing altered mental status

Outcomes

Primary Outcomes

Pain Score

Time Frame: 48 hours

We will assess a pain score based on a visual analog score of 1-10 at 48 hours post operatively.

Secondary Outcomes

  • blood loss(6 hours)
  • analgesic use(7 days)
  • Anti emetic use(48 hours)
  • operative time(24 hours)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (8)

Loading locations...

Similar Trials

Lavage and Suction of the Right Upper... | Clinical Trial