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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


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

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