IV Acetaminophen for Postoperative Pain After Pelvic Organ Prolapse Repair

Completed · Phase 4 · Has a placebo group

Conditions studied: Pelvic Organ Prolapse

In brief

The purpose of this study is to determine whether preoperative IV Acetaminophen reduces postoperative pain and narcotic consumption in women undergoing surgical repair of pelvic organ prolapse.

Key facts

Study ID

NCT02155738

Run by

Halina M Zyczynski, MD

People needed

204

Starts

2014-07-01

Expected to finish

2017-08-31

Last updated by the study team

2018-11-19

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women ≥ 18 years of age
• scheduled to undergo surgery for POP via a vaginal or minimally invasive (laparoscopic/robotic) route at the University of Pittsburgh Medical Center
• women anticipated to have a hospital stay ≥24 hours

You may not qualify if…

• allergy/intolerance to acetaminophen
• hepatic dysfunction
• significant alcohol use - defined as patient reported consumption of more than 7 standard drinks per week and/or 3 drinks per day

Where it is running

• Magee-Womens Hospital of the University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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