Comparing opioid prescribing methods for laparoscopic gynecologic surgery
Prospective Study of Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery
This study tests whether using a special calculator for prescribing pain medication can help women recovering from laparoscopic hysterectomy manage their pain better than standard methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 12 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | Female |
| Sponsor | University of Tennessee Academic / other |
| Locations | 1 site (Memphis, Tennessee) |
| Trial ID | NCT06532708 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of the Opioid Calculator developed by the University of Michigan in determining appropriate opioid prescriptions for patients undergoing laparoscopic hysterectomy. Participants will be randomly assigned to receive either standard opioid prescribing practices or prescriptions based on the calculator's recommendations. The study will involve monitoring postoperative pain levels and tracking the number of opioid pills consumed by patients. Data will be collected through follow-up assessments at specified intervals after surgery to assess pain management and medication usage.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 to 80 who are scheduled for a laparoscopic hysterectomy as a day surgery.
Not a fit: Patients undergoing non-laparoscopic unplanned surgical procedures or those with a history of opioid use disorder will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more accurate opioid prescribing, potentially reducing the number of pills prescribed and minimizing the risk of opioid misuse.
How similar studies have performed: Other studies have shown promise in using structured tools for opioid prescribing, suggesting that this approach may be beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women aged 18 to 80 * Undergoing planned laparoscopic hysterectomy as a day surgery procedure Exclusion Criteria: * 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
Where this trial is running
Memphis, Tennessee
- University of Tennessee Health Science Center — Memphis, Tennessee, United States (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.