Fetal Neurobehavioral Development in Methadone Maintained Pregnancies

Status Completed

Clinical Trial Summary

The purpose of this study is to examine differences in fetal neurobehavior at peak (2 hours after oral dose) vs. trough (2 hours before oral dose) maternal plasma methadone levels.

Clinical Trial Description

This study will examine differences in fetal neurobehavior at peak (2 hours after oral dose) vs. trough (2 hours before oral dose) plasma methadone levels. Anecdotal clinical observations suggest that fetal activity is increased at trough methadone levels and decreased at peak methadone levels, yet the investigators do not understand how in utero methadone exposure affects fetal neurobehavioral state development. ;

Study Design

Related Conditions & MeSH terms

Opioid-Related Disorders

Clinical Trial Details

NCT number	NCT00067184
Study type	Observational
Source	Johns Hopkins University
Contact
Status	Completed
Phase
Start date	September 2002
Completion date	August 2010

View Details

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