Acamprosate for Treatment of Compulsive Behaviors and Craving in Parkinson's Disease
NCT ID: NCT00640952
Last Updated: 2015-11-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2006-08-31
2008-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Interventions
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acamprosate
333 mg 2 tabs tid
Eligibility Criteria
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Inclusion Criteria
2. Active dopaminergic therapy at stable dose for one month (levodopa or dopamine agonist)
3. Able and willing to complete Rating Scales
4. Presence of one or more compulsive behavior based on responses to Rating Scales (defined as \>5 on the SOGS; \>17 on the YBOCS-SV and YBOCS-CUV; \>1.7 on the SCS for women and \>2.1 on the SCS for men; \>15 on the YBOCS-BE, \>5.5 on the CQ).
5. Written informed consent
1. No significant psychiatric disease
2. Able and willing to complete Rating Scales
3. Written informed consent
Exclusion Criteria
2. Current participation in another clinical study
3. History of unstable psychiatric disease (as determined by the Principal Investigator)
4. Women of childbearing age not using appropriate contraceptive methods (oral contraceptives, condoms, surgery)
18 Years
ALL
Yes
Sponsors
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National Parkinson Foundation
OTHER
Baylor College of Medicine
OTHER
Responsible Party
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Joohi Jimenez-Shahed
Principal Investigator
Principal Investigators
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Joohi Jimenez-Shahed, MD
Role: PRINCIPAL_INVESTIGATOR
Baylor College of Medicine
Locations
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PDCMDC 6550 Fannin, Suite 1801
Houston, Texas, United States
Countries
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Related Links
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Parkinson's Disease Center and Movement Disorders Clinic
Other Identifiers
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H-19781
Identifier Type: -
Identifier Source: org_study_id
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