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NCT03369613 · ClinicalTrials.gov registry record · NA
Transcranial Electrical Stimulation for Cervical Dystonia
A NA study of Primary Cervical Dystonia, sponsored by University of Colorado, Denver.
- Completed
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT03369613 is a NA study of Primary Cervical Dystonia that has completed, run by University of Colorado, Denver. The registered enrollment target is 36 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03369613, a NA study of Primary Cervical Dystonia, has completed, sponsored by University of Colorado, Denver.
- COMPLETED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
There are two phases. Phase I: A single visit which includes a screening, clinical scales, and a MRI scan with simultaneous tES/sham tES in a randomized block design. Enrolls both Cervical Dystonia (CD) patients and healthy controls. Phase II: 5 consecutive days of 30-90 min visits to campus for tES or sham tES. Transcranial magnetic stimulation (TMS) measures and clinical scales will also be included on Day 1 and Day 5 visits. Enrolls only CD patients.
Conditions Studied
Interventions
- DEVICE transcranial electrical stimulation
Study Locations (1)
Colorado
- University of Colorado Denver - Aurora
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2017-10-27 |
| Est. Completion | 2021-09-20 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03369613
The ClinicalTrials.gov registry entry for NCT03369613 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Primary Cervical Dystonia appearing as the primary indexed condition, and to 1 intervention - of which transcranial electrical stimulation is the first listed.
NCT03369613 reports 1 study location spanning 1 distinct geographic area - top geographies include Colorado.
Frequently Asked Questions
What is clinical trial NCT03369613 about?
NCT03369613 is a clinical study titled "Transcranial Electrical Stimulation for Cervical Dystonia". There are two phases. Phase I: A single visit which includes a screening, clinical scales, and a MRI scan with simultaneous tES/sham tES in a randomized block design. Enrolls both Cervical Dystonia (CD) patients and healthy controls. Phase II: 5 consecutive days of 30-90 min visits to campus for t...
What is the current status of trial NCT03369613?
This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2017-10-27. Estimated completion is 2021-09-20.
What conditions does trial NCT03369613 study?
This clinical trial studies the following conditions: Primary Cervical Dystonia.
What interventions are being tested in trial NCT03369613?
The interventions under investigation include: transcranial electrical stimulation (DEVICE).
Who is sponsoring clinical trial NCT03369613?
This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03369613 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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