Grants and Contracts Details
Description
The primary objective of this trial is to evaluate the impact of treating opioid use
disorder (OUD) in pregnant women with extended-release (XR) buprenorphine (BUP) compared to sublingual
(SL) BUP on mother and infant outcomes.
The primary hypotheses are that the BUP-XR, relative to the BUPSL,
group will have significantly:
1) less illicit opioid use during pregnancy;
2) shorter infant hospital length of stay (LOS); and
3) greater postpartum BUP adherence. Testing conceptual models of the mechanisms by which
BUP-XR may improve mother-infant outcomes, relative to BUP-SL, is a secondary trial objective.
Status | Finished |
---|---|
Effective start/end date | 6/1/18 → 5/31/20 |
Funding
- University of Cincinnati: $39,251.00
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