WithdrawnNot applicableNCT01986764
E2 and LDX for the Treatment of Cognitive Complaints After Oophorectomy
Studying Infantile neuroaxonal dystrophy
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 Pennsylvania
- Principal Investigator
- C. Neill Epperson, MDUniversity of Pennsylvania
- Intervention
- Lisdexamfetamine(drug)
- Eligibility
- 30-48 years · FEMALE
- Timeline
- 2013 – 2013
Study locations (1)
- Penn Center for Women's Behavioral Wellness, Philadelphia, Pennsylvania, United States
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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