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Completed Phase 3 Interventional Results available

Randomized, Placebo-Controlled Study of AbobotulinumtoxinA (Dysport®) for the Treatment of Cervical Dystonia

ClinicalTrials.gov ID: NCT00257660

Public ClinicalTrials.gov record NCT00257660. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Multicentre, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Dysport® for the Treatment of Cervical Dystonia

Study identification

NCT ID
NCT00257660
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ipsen
Industry
Enrollment
116 participants

Conditions and interventions

Interventions

  • Botulinum toxin type A Biological
  • Placebo Drug

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 9, 2005
Primary completion
Aug 31, 2006
Completion
Aug 31, 2006
Last update posted
Sep 27, 2022

2005 – 2006

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
St. Joseph's Hospital and Medical Center Phoenix Arizona
Parkinson's and Movement Disorder Institute Fountain Valley California
USC School of Medicine Los Angeles California 90033
University of Florida Gainesville Florida
University of Miami Miami Florida
Emory University Atlanta Georgia
Rush University Medical Center Chicago Illinois
University of Iowa Iowa City Iowa
University of Maryland Medical Center Baltimore Maryland
Wayne State University Medical Center Southfield Michigan
Albany Medical Center Albany New York
Beth Israel Medical Center New York New York 10003
Columbia University New York New York
Wake Forest University Winston-Salem North Carolina
Allegeheny General Pittsburgh Pennsylvania
University of Texas Southwest Dallas Texas
Baylor College of Medicine Houston Texas
Swedish Neuroscience Seattle Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00257660, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 27, 2022 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00257660 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →