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NCT00895063 · ClinicalTrials.gov registry record · NA
Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia
A NA study, sponsored by NYU Langone Health.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT00895063 is a NA study that was terminated before completion, run by NYU Langone Health. The registered enrollment target is 8 participants.
The verdict
NCT00895063, a NA study, was terminated before completion, sponsored by NYU Langone Health.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
Studies have suggested that voluntary muscle exercise in the hand and face after botulinum toxin injection may enhance the clinical effects of the toxin. Exercise may speed up the absorption of the toxin by the nerves and enhance the clinical response. This study will explore the effect of exercise on botulinum toxin injections for spasmodic dysphonia (SD).
Interventions
- BEHAVIORAL Vocal Exercise
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2007-12 |
| Est. Completion | 2013-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00895063
The ClinicalTrials.gov registry entry for NCT00895063 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Vocal Exercise is the first listed.
NCT00895063 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00895063 about?
NCT00895063 is a clinical study titled "Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia". Studies have suggested that voluntary muscle exercise in the hand and face after botulinum toxin injection may enhance the clinical effects of the toxin. Exercise may speed up the absorption of the toxin by the nerves and enhance the clinical response. This study will explore the effect of exercise ...
What is the current status of trial NCT00895063?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2007-12. Estimated completion is 2013-05.
What interventions are being tested in trial NCT00895063?
The interventions under investigation include: Vocal Exercise (BEHAVIORAL).
Who is sponsoring clinical trial NCT00895063?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
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