CompletedNot applicableNCT03417583
Assessing Efficacy of Neuropsychiatric Assessment and Treatment Protocols in Huntington's Disease Patients
Studying Huntington disease
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
- Vanderbilt University Medical Center
- Principal Investigator
- David IsaacsVanderbilt University Medical Center
- Intervention
- Protocol Intervention Group(other)
- Enrollment
- 100 enrolled
- Eligibility
- 21 years · All sexes
- Timeline
- 2018 – 2023
Study locations (1)
- Vanderbilt Medical Center, Nashville, Tennessee, United States
Collaborators
Teva Pharmaceuticals USA
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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