Clinical Trials Directory

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

TypeNameDescription
DRUGAmlodipine 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.