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N/A Completed N=174 Randomized Single-blind Treatment

Expectations and Pain Control Advancement In surgeRy: The REPAIR Trial

Abuses Over-The-Counter/Prescription Medications · Pain, Postoperative · Opioid Use Disorder · Physical Activity
Source: ClinicalTrials.gov NCT03726476 ↗
Enrolled (actual)
174
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcomePrimary: Opioid Use at Approximately Two Weeks Post-op — 15; 22.5 MME

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.

Outcome Measures

OutcomeResultp-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

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)
View full record on ClinicalTrials.gov →

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. Informational only — not medical advice.

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