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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 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.

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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.

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

FieldValue
Enrollment Target 20 participants
Start Date 2015-10-28
Est. Completion 2020-03-03
Phase NA

What the Registry Record Tells You About NCT02334683

The ClinicalTrials.gov registry entry for NCT02334683 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 89-participant average among 8 other Spasticity trials with a reported enrollment target (78% lower). The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 708 total studies on file at ClinicalTrials.gov.

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 2 study locations spanning 2 distinct geographic areas - top geographies include 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.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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