RecruitingEarly Phase 1NCT06617949

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.


Sponsor

Medical College of Wisconsin

Enrollment

20 participants

Start Date

Jan 16, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Epidural local anesthetic infusion, a drug called Hydromorphone Patient Controlled Analgelsic, and others for people with substance use disorder (sud). The study is currently recruiting participants at 2 locations. People eligible for this study include women aged 18 Years to 40 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRegional Anesthesia

Transverse abdominal Plane(TAP) Block with long acting Exparel placed by a regional anesthesiologist.

DRUGHydromorphone Patient Controlled Analgelsic

This group will be administered epidural PCA as a modality for pain control post cesarian section

PROCEDUREEpidural local anesthetic infusion

Epidural group will receive pain control via a local anesthetic intermediate bolus infusion


Locations(2)

Froedtert Hospital Milwaukee, Wisconsin 53226

Milwaukee, Wisconsin, United States

Froedtert Hospital

Milwaukee, Wisconsin, United States

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NCT06617949


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