Skip to content

Predicting and Preventing Adverse Maternal and Child Outcomes of Opioid Use Disorder in Pregnancy

Predicting and Preventing Adverse Maternal and Child Outcomes of Opioid Use Disorder in Pregnancy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05942313
Enrollment
100
Registered
2023-07-12
Start date
2023-08-28
Completion date
2026-12-01
Last updated
2026-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Use Disorder, Pregnancy Related

Brief summary

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.

Detailed description

Background: 7% of pregnant women in the U.S. use opioids and 21% of these women report misuse, making opioid use disorder (OUD) a major public health concern during pregnancy. The number of infants born with prenatal opioid exposure, neonatal opioid withdrawal syndrome (NOWS) and costly prolonged hospitalization has increased exponentially. The opioid epidemic is further worsened by the ongoing COVID-19 pandemic. Despite medication treatment for OUD with buprenorphine (BUP) or methadone (METH), these pregnant women continue to be at high risk for early relapse, polysubstance use, and depression. These infants are at risk for not only immediate NOWS and also poor long-term neurodevelopmental and behavioral outcomes. Genetic factors influence 30-60% of opioid adverse events (AEs). In pregnant women on medication management for OUD, and infants receiving opioids for NOWS treatment there is variability in dose required to prevent withdrawal symptoms and craving, likely related to physiological alterations, upregulation of metabolic and biological pathways, determined in part by opioid pharmacogenomics. Investigators have shown that in children and adults, opioid related poor clinical outcomes are related to opioid receptor genetic variations and resulting variations in their metabolism. Maternal depression and anxiety increase the risks for OUD, maternal relapse, NOWS and negatively impact pregnant women and their children. Thus, there is an urgent and unmet clinical need for a reliable tool to proactively predict maternal relapse, NOWS, and improve the safety of pregnant women with OUD and their children.

Interventions

DRUGBuprenorphine/ Methadone exposure

Validate candidate genes- and prenatal opioid exposure- related maternal relapse and NOWS outcome associations in pregnant women and their newborns.

Sponsors

Ilana Hull
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
OpalGenix, Inc
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pregnant women with OUD and their infant * Currently on BUP/METH for OUD * Enrolled in prenatal opioid maintenance program * Age \>18 years * Singleton pregnancy * Planned delivery at UPMC's Magee Womans Hospital * Positive opioid urine screen results

Exclusion criteria

* Serious maternal medical illness as deemed by the PI that would make it challenging to comply with study procedures * HIV or AIDS * Known major fetal congenital abnormalities

Design outcomes

Primary

MeasureTime frameDescription
Incidence of maternal opioid relapseMeasured from enrollment to 3-months post deliveryMeasured via binary response, yes/no
Incidence of NOWSMeasured at deliveryClinical definition of NOWS: Substance withdrawal encompasses a continuum of variable clinical expression from neonate to neonate; the diagnosis is not limited only to neonates who require pharmacotherapy. Incidence of NOWS measured by binary response, yes/no

Secondary

MeasureTime frameDescription
Severity of Maternal Opioid RelapseMeasured from enrollment to 3-months post deliverySeverity of maternal opioid relapse measured by requirement of medical treatment (binary response, yes/no)
Severity of NOWsMeasured at deliverySeverity of NOWs measured by the need for \>3 days of hospital stay (binary response, yes/no)

Countries

United States

Contacts

CONTACTAmy Monroe, MPH, MBA
monroeal@upmc.edu412-623-6382
CONTACTCarly Riedmann, MPH
riedmannca@upmc.edu412-623-4147
PRINCIPAL_INVESTIGATORIlana Hull, MD

Univrsity of Pittsburgh / UPMC Magee Womens Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 7, 2026