Citalopram to Enhance Cognition in HD
NCT00271596 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 33
Last updated 2013-03-13
Summary
This research plan proposes to conduct a double-blind, placebo-controlled pilot clinical trial in 36 adults with mild Huntington's disease (HD) to address the following research aims:
1. To determine the effect of citalopram compared to placebo in patients with early HD on executive function and other outcome variables including functional measures (health-related quality of life, work productivity, and self-reported attention), motor performance, and psychiatric status,
2. To study the relationship between executive function and functional status in patients with early HD after selective serotonin reuptake inhibitor (SSRI) treatment, and
3. To examine the effect of citalopram treatment on volumetric and metabolic (i.e, N-acetyl-aspartate concentration) measures in the neostriatum among patients with recently diagnosed Huntington's disease.
Conditions
- Huntington Disease
- Chorea
- Executive Dysfunction
Interventions
- DRUG
-
20mg daily citalopram
a selective serotonin reuptake inhibitor (SSRI) treatment administered over 16 weeks
- DRUG
-
a daily matching placebo administered over 16 weeks
Sponsors & Collaborators
-
National Institute of Neurological Disorders and Stroke (NINDS)
collaborator NIH -
Cure Huntington's Disease Initiative (CHDI)
collaborator UNKNOWN -
University of Rochester
collaborator OTHER - collaborator OTHER
-
University of Iowa
lead OTHER
Principal Investigators
-
Leigh J Beglinger, Ph.D. · The University of Iowa Psychiatry Department
-
Jess G Fiedorowicz, M.D., Ph.D. · University of Iowa Psychiatry Department
-
Kevin Biglan, M.D., M.P.H. · University of Rochester
-
John Caviness, M.D. · Mayo Clinic
-
Ricardo Jorge, M.D. · University of Iowa Psychiatry Department
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-11-30
- Primary Completion
- 2011-04-30
- Completion
- 2011-11-30
Countries
- United States
Study Locations
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