Actively Recruiting
Predicting and Preventing Adverse Maternal and Child Outcomes of Opioid Use Disorder in Pregnancy
Led by Ilana Hull · Updated on 2026-03-19
100
Participants Needed
1
Research Sites
170 weeks
Total Duration
On this page
Sponsors
I
Ilana Hull
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study will be a 12-month prospective, genotype-blinded longitudinal observational study with current standard of clinical care. This study will enroll 100 pregnant women with OUD at UPMC Hospitals with its high volumes. Because of the observational nature of the study, the anticipated dropout rate will be ≤ 20%. Investigators expect the effective sample size of evaluable patients will be 200 with longitudinal data.
CONDITIONS
Official Title
Predicting and Preventing Adverse Maternal and Child Outcomes of Opioid Use Disorder in Pregnancy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women with opioid use disorder (OUD) and their infant
- Currently on buprenorphine or methadone treatment for OUD
- Enrolled in a prenatal opioid maintenance program
- Age greater than 18 years
- Singleton pregnancy
- Planned delivery at UPMC's Magee Womans Hospital
- Positive opioid urine screen results
You will not qualify if you...
- Serious maternal medical illness making study participation difficult
- HIV or AIDS infection
- Known major fetal congenital abnormalities
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UPMC Magee-Womens Hospital
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
Research Team
A
Amy Monroe, MPH, MBA
CONTACT
C
Carly Riedmann, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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