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Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications.
Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications: Efficacy and Safety Outcomes.
Who can join
Ages 18 to 40 · Women
Full eligibility criteria
Inclusion Criteria: * Inclusion criteria include being a parturient with Substance use disorder (SUD) and age 18-35 Exclusion Criteria: * Exclusion criteria include having a diagnosed medical condition(allergies to medication, pathology such as severe aortic stenosis excluding patients from receiving an epidural etc) that will exempt patient from intervention arm of the study.
About the study
The purpose of this study is to investigate the efficacy of three different modalities of post-operative pain control in parturient with opioid use disorders. The investigators aim to determine whether the different approach utilized show better outcomes with pain management and if there are any association with reduction of symptoms of anxiety, depression, and overall well-being.
What is being tested
- Regional Anesthesia (drug)
- Hydromorphone Patient Controlled Analgelsic (drug)
- Epidural local anesthetic infusion (procedure)
Sponsor: Medical College of Wisconsin · Participants: 20 · Started: Jan 16, 2025
Contact the study team
- Meredith Albrecht, MD, PhD · Phone: 414-805-8700
- Christopher Fadumiye, MD · Phone: 414-805-8700
Official record on ClinicalTrials.gov — NCT06617949
Locations in the U.S.
| Wisconsin | Froedtert Hospital, Milwaukee (Not yet recruiting) Froedtert Hospital Milwaukee, Wisconsin 53226, Milwaukee |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.