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Clinical Trial Summary

The safety and efficacy of Mentor Purified Toxin, Botulinum Toxin Type A, Purified Neurotoxin, injected intramuscularly into the neck, is being evaluated as a treatment for painful and non-painful spasmodic torticollis/cervical dystonia. It is hypothesized that treatment will decrease symptom severity and will not have any significant side effects.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00549341
Study type Interventional
Source Mentor Worldwide, LLC
Contact
Status Completed
Phase Phase 1
Start date May 2006
Completion date March 2009

See also
  Status Clinical Trial Phase
Completed NCT00528541 - Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Type A in Moderate to Severe Cervical Dystonia Phase 4
Completed NCT00210431 - Post Marketing Surveillance Study of Dysport
Completed NCT03471923 - Non-Motor Features of Cervical Dystonia (CD)
Completed NCT01859247 - Identification of Optimal Stimulation Site for Cervical Dystonia Symptoms: An Exploratory Study N/A
Terminated NCT00432341 - Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Moderate to Severe Cervical Dystonia Phase 4
Completed NCT00165776 - Randomized, Double-Blind, Placebo-Controlled, Parallel, Group Dose-Response, Study of E2014 in Patients WIth Spasmodic Torticollis Phase 2
Completed NCT00280384 - An Electrophysiological Study Of E2014 In Healthy Adult Male Japanese And Caucasian Subjects Phase 2