CompletedPhase 1NCT00417794
Assess the Effectiveness of Atomoxetine in Children With Fetal Alcohol Syndrome and ADD/ADHD
Studying Fetal alcohol syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Oklahoma
- Principal Investigator
- Laura J McGuinn, PhDUniversity of Oklahoma
- Intervention
- Strattera(drug)
- Enrollment
- 38 enrolled
- Eligibility
- 4-11 years · All sexes
- Timeline
- 2005 – 2015
Study locations (1)
- OU Child Study Center, Oklahoma City, Oklahoma, United States
Collaborators
Mark L. Wolraich, M.D. · Eli Lilly and Company
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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