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NCT02334683 · ClinicalTrials.gov registry record · NA
Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatment of Limb Spasticity and Focal Dystonia
A NA study of Spasticity and Focal Dystonia, sponsored by Icahn School of Medicine at Mount Sinai.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 2
- Study locations
NCT02334683: Completed NA study of Spasticity and Focal Dystonia, sponsored by Icahn School of Medicine at Mount Sinai.
NCT02334683 is a NA study of Spasticity and Focal Dystonia that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 20 participants, below the 89-participant average among 8 other Spasticity trials with a reported enrollment target (78% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02334683, a NA study of Spasticity and Focal Dystonia, has completed, sponsored by Icahn School of Medicine at Mount Sinai.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 2
- Study locations
Study Summary
This study seeks to compare the use of ultrasound and electrophysiologic techniques to target muscles for the treatment of spasticity and focal dystonia of the limbs. The purpose of this study is to investigate the use of two ways of locating the muscle for botulinum toxin (BoNT) injection for the treatment of focal hand dystonia and upper limb spasticity. Electrophysiologic guidance, using electrical stimulation, and ultrasound are the standard ways of locating muscles during a treatment of BoNT injection.
Primary Outcome
clinical or patient self-rating form for grading evaluation of the treatment at 16 weeks as compared to at 4 weeks. Full scale from 0 = no improvement and 100 normal use. Higher score indicates better health outcome.
Conditions Studied
Interventions
- DEVICE Ultrasound
- DEVICE Electrical stimulation
Study Locations (2)
Maryland
- Ninds, Nih - Bethesda
New York
- Icahn School of Medicine at Mount Sinai - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2015-10-28 |
| Est. Completion | 2020-03-03 |
| Phase | NA |
What the finished NCT02334683 record still lists
NCT02334683 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 89-participant average among 8 other Spasticity trials with a reported enrollment target (78% lower).
The record links to 3 conditions, with Spasticity appearing as the primary indexed condition, and to 2 interventions - of which Ultrasound is the first listed.
NCT02334683 reports a single indexed study location in Maryland, New York.
Frequently Asked Questions
What is clinical trial NCT02334683 about?
NCT02334683 is a clinical study titled "Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatment of Limb Spasticity and Focal Dystonia". This study seeks to compare the use of ultrasound and electrophysiologic techniques to target muscles for the treatment of spasticity and focal dystonia of the limbs. The purpose of this study is to investigate the use of two ways of locating the muscle for botulinum toxin (BoNT) injection for the t...
What is the current status of trial NCT02334683?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2015-10-28. Estimated completion is 2020-03-03.
What conditions does trial NCT02334683 study?
This clinical trial studies the following conditions: Spasticity, Focal Dystonia, Tremor, Limb.
What interventions are being tested in trial NCT02334683?
The interventions under investigation include: Ultrasound (DEVICE), Electrical stimulation (DEVICE).
Who is sponsoring clinical trial NCT02334683?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02334683 being conducted?
This trial has 2 study locations across Maryland, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02334683's enrollment target sits among peer trials
20 5th of 8 higher than 4 of 8 other Spasticity trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Spasticity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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