Grants and Contracts Details
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.
|Effective start/end date||6/1/18 → 5/31/20|
- University of Cincinnati: $39,251.00
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