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NCT04916444 · ClinicalTrials.gov registry record · NA
Dystonia Treatment With Injections Supplemented By Transcranial Magnetic Stimulation
A NA study, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 5
- Enrollment target
NCT04916444 is a NA study that has completed, run by University of Florida. The registered enrollment target is 5 participants.
The verdict
NCT04916444, a NA study, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 5 participants
- Enrollment target
Study Summary
We applied 16 sessions of rTMS over 4 consecutive days for adult patients suffering from cervical dystonia who received botulinum toxin (BoNT) injections on a regular basis. The TMS protocol took place 9 weeks following their last BoNT injection. The primary outcome measure was improvement in cervical dystonia as measured by the TWSTRS scale. The secondary outcome measures included mood, cognition, and gait measures.
Interventions
- DEVICE rTMS
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2022-02-07 |
| Est. Completion | 2024-01-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04916444
The ClinicalTrials.gov registry entry for NCT04916444 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which rTMS is the first listed.
NCT04916444 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04916444 about?
NCT04916444 is a clinical study titled "Dystonia Treatment With Injections Supplemented By Transcranial Magnetic Stimulation". We applied 16 sessions of rTMS over 4 consecutive days for adult patients suffering from cervical dystonia who received botulinum toxin (BoNT) injections on a regular basis. The TMS protocol took place 9 weeks following their last BoNT injection. The primary outcome measure was improvement in cervic...
What is the current status of trial NCT04916444?
This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2022-02-07. Estimated completion is 2024-01-07.
What interventions are being tested in trial NCT04916444?
The interventions under investigation include: rTMS (DEVICE).
Who is sponsoring clinical trial NCT04916444?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
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