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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04049799
Other study ID # STUDY00000166
Secondary ID R01DA047867
Status Completed
Phase
First received
Last updated
Start date August 8, 2019
Est. completion date February 1, 2024

Study information

Verified date February 2024
Source University of Vermont
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will compare medically-supervised withdrawal (MSW, 'detoxification') to opioid agonist treatment (OAT, 'maintenance') with buprenorphine for pregnant women with opioid use disorder in terms of maternal, fetal, and neonatal outcomes. Outcomes will be assessed during pregnancy, at birth and for 12 months postpartum. This study has the potential to impact health service policy and practices in terms of the treatment options of pregnant women with opioid use disorder.


Description:

Some inclusion/exclusion criteria are purposely omitted at this time to preserve scientific integrity. They will be included after the trial is complete.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date February 1, 2024
Est. primary completion date February 1, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 41 Years
Eligibility Inclusion Criteria: - Be ages 18 to 41, inclusive - Have a single fetus pregnancy between 6-30 weeks estimated gestational age - Willing to participate in the study Exclusion Criteria: - Non-English speaking

Study Design


Intervention

Other:
Medically-supervised withdrawal
6-8 day withdrawal with buprenorphine/naloxone
Opioid agonist treatment
Induction and maintenance with buprenorphine/naloxone
Behavioral:
Comprehensive clinical care
Obstetrical visits, counseling, case management, psychiatry services, and urine drug screening

Locations

Country Name City State
United States Mountain Area Health Education Center Asheville North Carolina
United States University of Vermont Burlington Vermont
United States UNC Chapel Hill Horizons Chapel Hill North Carolina
United States Virginia Commonwealth University Richmond Virginia

Sponsors (6)

Lead Sponsor Collaborator
University of Vermont Johns Hopkins University, Mountain Area Health Education Center, National Institute on Drug Abuse (NIDA), University of North Carolina, Chapel Hill, Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of mothers who discontinued 1st treatment choice prior to delivery Antepartum period
Primary Proportion of mothers engaged in treatment at delivery Behavior health treatment or medical treatment in past 21 days Antepartum period
Primary Proportion of mothers with illicit substance use at delivery Positive vs. negative for any illicit substance in the urine At delivery
Primary Proportion of mother-child dyads with delivery complications Yes vs. no code for the presence or absence of delivery complications such as uterine rupture, placental abruption, low birth weight, chorioamnionitis, and meconium staining At delivery
Primary Proportion of neonates receiving medication treatment for neonatal abstinence syndrome (NAS) Yes vs. no At hospital discharge, an average of 10 days after delivery
Primary Total average amount of medication given to treat NAS Morphine Equivalent Dose in mg At hospital discharge, an average of 10 days after delivery
Primary Total average length of neonatal hospital stay Days At hospital discharge, an average of 10 days after delivery
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