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

Inclusion Criteria2

  • Women aged 18 to 80
  • Undergoing planned laparoscopic hysterectomy as a day surgery procedure

Exclusion Criteria3

  • Women aged 18 to 80
  • Undergoing a non-laparoscopic unplanned surgical procedure
  • Patients with a history of opioid use disorder or current opioid use disorder

Interested in this trial?

Get notified about updates and connect with the research team.

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

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06532708


Related Trials