Trials / Completed
CompletedNCT00015457
Amlodipine Plus Botulinum Toxin for Focal Dystonia
Trial of Amlodipine Combined With Botulinum Toxin Injections for Focal Dystonia
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 16 (actual)
- Sponsor
- National Institute of Neurological Disorders and Stroke (NINDS) · NIH
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Objective: To determine if the calcium channel blockers, amlodipine can augment the effect of botulinum toxin injections in the treatment of focal dystonia. Study Population: 20 patients with cervical dystonia Design: Double-bind, placebo-controlled clinical trail. Outcome measures: For patients: dystonia rating scales (Twistrs, Fahn-Marsden dystonia scale, NINDS subjective patient rating scale), and hand grip strength. For healthy volunteers: Amplitude of EDB MEP.
Detailed description
Objective: To determine if the calcium channel blocker, amlodipine can augment the effect of botulinum toxin injections in the treatment of focal dystonia. Study Population: 20 patients with cervical dystonia Design: Double-bind, placebo-controlled clinical trail. Outcome measures: dystonia rating scales (TWISTRS)
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Amlodipine plus Botulinum toxin |
Timeline
- Start date
- 2001-04-01
- Primary completion
- 2009-04-01
- First posted
- 2001-04-19
- Last updated
- 2013-04-01
- Results posted
- 2013-04-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00015457. Inclusion in this directory is not an endorsement.