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Nicotinic Acetylcholine Receptor Agonist
Nicotine patch for Parkinson's Disease
Phase 4
Waitlist Available
Led By James Boyd, MD
Research Sponsored by University of Vermont
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12-20 minutes
Awards & highlights
Study Summary
The specific aims of this study are to examine whether treatment with transdermal nicotine improves computer-based laboratory and clinical measures of impulsive and compulsive behaviors in Parkinson's Disease subjects who have recently experienced an impulse control disorder.
Eligible Conditions
- Parkinson's Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12-20 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12-20 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Stop Signal task
Secondary outcome measures
Set shifting task
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Nicotine patchActive Control1 Intervention
Group II: Placebo patchPlacebo Group1 Intervention
Find a Location
Who is running the clinical trial?
University of VermontLead Sponsor
266 Previous Clinical Trials
3,743,671 Total Patients Enrolled
Parkinson's Disease FoundationOTHER
9 Previous Clinical Trials
817 Total Patients Enrolled
The Parkinson Study GroupNETWORK
15 Previous Clinical Trials
21,985 Total Patients Enrolled
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