Fetal Neurobehavioral Development in Methadone Maintained Pregnancies

NCT00067184 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 157

Last updated 2018-04-25

No results posted yet for this study

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.

Conditions

  • Opioid-Related Disorders

Interventions

DEVICE

Toitu 320/325

Fetal monitor

Sponsors & Collaborators

Principal Investigators

  • Lauren M. Jansson, M.D. · Johns Hopkins University

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-09-30
Primary Completion
2010-08-31
Completion
2010-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00067184 on ClinicalTrials.gov