MedPath

Pain With Differing Insufflation Pressures During Laparoscopic Hysterectomy

Not Applicable
Recruiting
Conditions
Post Operative Pain
Interventions
Procedure: Lower Insufflation Pressure
Procedure: Standard Insufflation Pressure
Registration Number
NCT06508814
Lead Sponsor
University of Tennessee
Brief Summary

The purpose of this study is to determine the effect of decreased insufflation pressure on postoperative pain, analgesic use, and surgical safety and feasibility for laparoscopic hysterectomy.

Detailed Description

This is a prospective, single-blinded, randomized clinical trial in which participants undergoing laparoscopic hysterectomy will be randomized in a 1:1 ratio to undergo surgery with peritoneal insufflation pressure set to 15 mmHg (standard) or 12 mmHg (comparison). Randomization was performed using computer-generated permuted blocks of four participants. All participants on the first postoperative day will be asked to rate their pain with a Visual Analog Scale (VAS). At a postoperative visit 2 weeks after surgery, all participants will be asked to complete the VAS again. The highest preoperative pain (up to 2 hours before surgery) and immediate postoperative pain, using the VAS, in the post anesthesia care unit (PACU) will be recorded. All participants will be planned for discharge from PACU. Age, body mass index, gynecologic diagnosis, medical history, and preoperative analgesia or opioid use will be extracted from the medical records by trained research staff and entered into a secure electronic database. Preoperative analgesia and opioid saw will be verified with active prescription records at the time of surgery. After surgery, analgesic doses, operative time, additional procedures performed, conversion to laparotomy or increased insufflation pressure, estimated blood loss, and length of stay will be recorded.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • Women aged 18 to 80
  • BMI 55.0 or less
  • Laparoscopic hysterectomy surgery planned
Exclusion Criteria
  • Women younger than 18 or older than 80 years of age
  • BMI over 55.0
  • Laparoscopic hysterectomy surgery not planned

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
12 mmHg Insufflation PressureLower Insufflation PressureParticipants received 12 mmHg of insufflation pressure during their laparoscopic hysterectomy.
15 mmHg Insufflation PressureStandard Insufflation PressureParticipants received 15 mmHg of insufflation pressure during their laparoscopic hysterectomy.
Primary Outcome Measures
NameTimeMethod
Pain on postoperative day 124 hours following surgery

All participants will be asked to rate their pain using the Visual Analog Scale (VAS) approximately 24 hours after surgery completion. This scale ranges from 0 to 10, with 0 indicating no pain and 10 indicating worst possible pain.

Secondary Outcome Measures
NameTimeMethod
Preoperative painWithin 2 hours before surgery

All participants will be asked to rate their pain using the Visual Analog Scale (VAS) upon their arrival before surgery. This scale ranges from 0 to 10, with 0 indicating no pain and 10 indicating worst possible pain.

Postoperative pain while in PACUApproximately 2 hours after surgery completion

All participants will be asked to rate their pain using the Visual Analog Scale (VAS) while they are recovering in PACU, approximately 2 hours after surgery completion. This scale ranges from 0 to 10, with 0 indicating no pain and 10 indicating worst possible pain.

Opioid use after dischargeWithin 2 weeks after surgery

All participants will be asked about the number of prescription opioid pills they took following discharge.

Postoperative pain at follow-up visitApproximately 2 weeks after surgery completion

All participants will be asked to rate their pain using the Visual Analog Scale (VAS) at their 2-week postoperative follow-up visit. This scale ranges from 0 to 10, with 0 indicating no pain and 10 indicating worst possible pain.

Trial Locations

Locations (1)

University of Tennessee Health Science Center

🇺🇸

Memphis, Tennessee, United States

© Copyright 2025. All Rights Reserved by MedPath