Short Title: Standard vs. Lower Pressure Pneumoperitoneum
ConditionLaparoscopic Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCedars-Sinai Medical Center
About this trial
This study aims to investigate the effect of varying insufflation pressures on post-operative pain and adequacy of surgical field visualization among patients undergoing laparoscopic surgery with a minimally invasive gynecologic surgeon.
Eligibility criteria
Qualifiers
Provision of signed and dated informed consent form
Stated willingness to comply with all study procedures and availability for the duration of the study
18 years of age or older
Undergoing laparoscopic surgery at Cedars-Sinai Medical Center with a surgeon in the Minimally Invasive Gynecologic Surgery division.
Disqualifiers
Pregnancy
Urgent/non-scheduled surgery
Scheduled for planned or possible concomitant non-gynecologic surgery (e.g., urologic or colorectal procedure)
Baseline opioid use
Trial design
Treatments tested in this trial
- Carbon dioxide
- Bupivacaine
- Oxycodone
Treatment groups
294 Participants
are divided into 6 treatment groups6
Treatment groupsSee each treatment group below.
Sponsors and collaborators
Source ClinicalTrials.gov