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NCT02046447 · ClinicalTrials.gov registry record
Neuroimaging of Dystonia
A clinical trial of Primary Cervical Dystonia and DYT 1 Dystonia, sponsored by University of Florida.
- Completed
- Registry status
- 20
- Enrollment target
- 1
- Study location
NCT02046447: Completed study of Primary Cervical Dystonia and DYT 1 Dystonia, sponsored by University of Florida.
NCT02046447 is a study of Primary Cervical Dystonia and DYT 1 Dystonia that has completed, run by University of Florida. The registered enrollment target is 20 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02046447, a study of Primary Cervical Dystonia and DYT 1 Dystonia, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The main purpose of this study is to investigate primary cervical dystonia as compared to healthy control subjects and DYT 1 dystonia as compared to healthy control subjects by examining cognitive measures, physical measures, and structural and functional magnetic resonance imaging (MRI). The secondary aim of this study is to investigate a specific drug therapy for primary cervical dystonia to develop a functional MRI (fMRI) research paradigm. The drug, trihexyphenidyl, is FDA approved to treat Parkinson's Disease and is commonly prescribed by physicians as a treatment for symptoms of primary cervical dystonia.
Primary Outcome
Participants will use their hand to squeeze an MRI compatible grip force transducer in the MRI unit. While producing force, the participants will observe the amount of force generated by viewing a visual feedback display.
Conditions Studied
Interventions
- DRUG Primary Cervical Dystonia (Trihexyphenidyl)
- OTHER Controls Primary Cervical Dystonia (Trihexyphenidyl)
- OTHER DYT 1 Dystonia (Healthy Control)
- OTHER DYT 1 Dystonia
Study Locations (1)
Florida
- University of Florida - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2014-05 |
| Est. Completion | 2017-12 |
What the finished NCT02046447 record still lists
NCT02046447 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.
The record links to 2 conditions, with Primary Cervical Dystonia appearing as the primary indexed condition, and to 4 interventions - of which Primary Cervical Dystonia (Trihexyphenidyl) is the first listed.
NCT02046447 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT02046447 about?
NCT02046447 is a clinical study titled "Neuroimaging of Dystonia". The main purpose of this study is to investigate primary cervical dystonia as compared to healthy control subjects and DYT 1 dystonia as compared to healthy control subjects by examining cognitive measures, physical measures, and structural and functional magnetic resonance imaging (MRI). The secon...
What is the current status of trial NCT02046447?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2014-05. Estimated completion is 2017-12.
What conditions does trial NCT02046447 study?
This clinical trial studies the following conditions: Primary Cervical Dystonia, DYT 1 Dystonia.
What interventions are being tested in trial NCT02046447?
The interventions under investigation include: Primary Cervical Dystonia (Trihexyphenidyl) (DRUG), Controls Primary Cervical Dystonia (Trihexyphenidyl) (OTHER), DYT 1 Dystonia (Healthy Control) (OTHER), DYT 1 Dystonia (OTHER).
Who is sponsoring clinical trial NCT02046447?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02046447 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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