Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery

Part of paid clinical trials in Memphis, Tennessee.

Sponsor
University of Tennessee
Study ID
NCT06532708
Status
Recruiting
Apply to this trial

Conditions

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 80 Years
Healthy Volunteers
Accepted

Interventions

  • 5x Oxycodone Oral Tablets — OTHER
    Participants will be prescribed 5 doses of 5mg tablets of oxycodone for postoperative pain relief.
  • 16x Oxycodone Oral Tablets — OTHER
    Participants will be prescribed 16 doses of 5mg tablets of oxycodone for postoperative pain relief.

Study Details

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.

Key Dates

Start date
Jul 12, 2024
Status verified
Jul 2024
Primary completion
Oct 31, 2024
Completion
Oct 31, 2024

Study Design

Enrollment
12 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: 5 Doses
    Participants will receive 5 doses of prescription opioids following surgery.
  • Active Comparator: 16 Doses
    Participants will receive 16 doses of prescription opioids following surgery.

Primary Outcome Measure

Number of pills used [ Time Frame: Within 1 week following surgery ]

Locations (1)

FacilityCityStateZIPSite coordinators
University of Tennessee Health Science CenterMemphisTennessee38103
Amira Wohabrebbi, PhD
[email protected]
901-545-7453
Annette Hickerson, RN
[email protected]
901-448-4784
John O Schorge, MD (PRINCIPAL_INVESTIGATOR)
Emma Ryan, BS (SUB_INVESTIGATOR)
Alex Samborski, MD (SUB_INVESTIGATOR)
Caroline Reidy, BS (SUB_INVESTIGATOR)
Rachel Nelson, MD (SUB_INVESTIGATOR)
Daniel Amram, BS (SUB_INVESTIGATOR)

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