RecruitingNot ApplicableNCT06532708

Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery

Prospective Study of Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery


Sponsor

University of Tennessee

Enrollment

12 participants

Start Date

Jul 12, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to compare opioid prescribing practices by either routine provider prescribing practices, or with the use of a calculator, i.e., the Opioid Calculator, published by the University of Michigan (www.opioidcalculator.org), with the intent of decreasing the number of pills.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying 16x Oxycodone Oral Tablets and 5x Oxycodone Oral Tablets for people with opioid use and postoperative pain. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 80 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHER5x Oxycodone Oral Tablets

Participants will be prescribed 5 doses of 5mg tablets of oxycodone for postoperative pain relief.

OTHER16x Oxycodone Oral Tablets

Participants will be prescribed 16 doses of 5mg tablets of oxycodone for postoperative pain relief.


Locations(1)

University of Tennessee Health Science Center

Memphis, Tennessee, United States

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NCT06532708


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