Clinical trial
Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving…
NCT00462449 · University of Pittsburgh, Other · Completed
Key facts
| NCT number | NCT00462449 |
|---|---|
| Title | Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving Botulinum Neurotoxin for Upper Extremity Spasticity |
| Official title | Single Blind, Randomized Study to Determine the Safety and the Efficacy of Using Functional Electrical Stimulation (FES) and Repetitive Task Practice vs. Repetitive Task Practice Alone in Persons Receiving Botulinum Neurotoxin Type A Injections for Upper Extremity Spasticity |
| Acronym | Botox + FES |
| Lead sponsor | University of Pittsburgh, Other |
| Collaborators | Allergan Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Upper Extremity Spasticity, Stroke, Acquired Brain Injury |
| Intervention type | Device |
| Interventions | Functional Electrical Stimulation (FES) through the Ness H200 |
| Enrollment | 23 |
| Start date | Nov 1, 2007 |
| Primary completion | Jan 1, 2010 |
| Completion | Jan 1, 2010 |
| First posted | Apr 19, 2007 |
| Last update posted | Jun 20, 2014 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About ClinicalTrials.gov studies
ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.
Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: