Perinatal Opioid Use

Status Completed

Clinical Trial Summary

To compare maternal and newborn outcomes among pregnant women with OUD receiving care via telemedicine versus in-person.

Clinical Trial Description

Participants: Pregnant women with OUD.

Intervention: Participants were seen weekly for four weeks, every two weeks for four weeks and monthly thereafter and provided relapse-prevention therapy and buprenorphine.

Design: A cohort derived from a prospectively collected database including 98 women receiving perinatal OUD treatment in an obstetric practice by telemedicine or in-person and followed until 6-8 weeks postpartum from September, 2017 to December, 2018. Logistic regression with propensity score adjustment was applied to reduce group selection bias and control for potentially confounding variables.

Setting: Four outpatient obstetric practices in the southeast. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04049032
Study type	Observational
Source	Medical University of South Carolina
Contact
Status	Completed
Phase
Start date	September 1, 2017
Completion date	December 31, 2018

View Details

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