Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications.

Description

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.

Conditions

Substance Use Disorder (SUD)

Study Overview

Study Details

Study overview

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.

Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications: Efficacy and Safety Outcomes.

Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications.

Condition
Substance Use Disorder (SUD)
Intervention / Treatment

-

Contacts and Locations

Milwaukee

Froedtert Hospital Milwaukee, Wisconsin 53226, Milwaukee, Wisconsin, United States, 53226

Milwaukee

Froedtert Hospital, Milwaukee, Wisconsin, United States, 53226

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Inclusion criteria include being a parturient with Substance use disorder (SUD) and age 18-35
  • * 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.

Ages Eligible for Study

18 Years to 40 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Medical College of Wisconsin,

Study Record Dates

2028-12