N/A
N=174
Expectations and Pain Control Advancement In surgeRy: The REPAIR Trial
Abuses Over-The-Counter/Prescription Medications · Pain, Postoperative · Opioid Use · Physical Activity · Patient Dependence on
Bottom Line
View on ClinicalTrials.gov: NCT03726476 ↗Enrolled (actual)
174
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: Opioid Use at Approximately Two Weeks Post-op — 15; 22.5 MME
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Patient centered pre-op education (Behavioral); routine preop education (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- University of New Mexico
- Primary completion
- Dec 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Opioid Use at Approximately Two Weeks Post-op |
15; 22.5 | — |
| SECONDARY Opioid Use at Approximately Six to Eight Weeks Post-op |
15; 23 | — |
Summary
This is a randomized control trial that aims to evaluate whether patient-centered education, compared to routine education, decreases narcotic consumption without interfering with return to physical activity following hospital discharge. In addition, it will test whether patient-centered education decreases the quantity of narcotics prescribed and/or increases patient satisfaction and preparedness.
Eligibility Criteria
Inclusion Criteria
- Subjects are ≥ 18 years of age
- English or Spanish speaking
- Patient scheduled for pelvic floor surgery
Exclusion Criteria
- Unable to speak English or Spanish
- Using long acting opioids (e.g. MS Contin, Fentanyl patch)
- Primary or Pain Healthcare Provider recommends against study participation (eg. If the patient has a history of opioid use disorder or other confounding problems, we will contact the Primary Care Provider or Pain Healthcare Provider for their recommendations regarding study participation)
Data sourced from ClinicalTrials.gov (NCT03726476). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.