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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00432341




Registration number
NCT00432341
Ethics application status
Date submitted
5/02/2007
Date registered
7/02/2007
Date last updated
16/12/2011

Titles & IDs
Public title
Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Moderate to Severe Cervical Dystonia
Scientific title
Secondary ID [1] 0 0
MedAff-BTX-0615
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Spasmodic Torticollis 0 0
Condition category
Condition code
Musculoskeletal 0 0 0 0
Other muscular and skeletal disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - botulinum toxin type A
Treatment: Other - botulinum toxin type A

Experimental: BOTOX® - Botulinum toxin type A (BOTOX®)

Active comparator: Dysport® - Botulinum toxin type A (Dysport®)


Treatment: Other: botulinum toxin type A
200 Units at Visit 1 (Day 1)

Treatment: Other: botulinum toxin type A
500 Units at Visit 1 (Day 1)
Intervention code [1] 0 0
Treatment: Other
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Duration of Treatment Benefit
Timepoint [1] 0 0
20 Weeks
Secondary outcome [1] 0 0
Toronto Western Spasmodic Torticollis Rating Scale Duration Target Score (TDTS) at Week 4
Timepoint [1] 0 0
Week 4
Secondary outcome [2] 0 0
Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) Total Score at Week 4
Timepoint [2] 0 0
Baseline, Week 4
Secondary outcome [3] 0 0
Global Assessment of Benefit by Patient at Week 4
Timepoint [3] 0 0
Week 4
Secondary outcome [4] 0 0
Global Assessment of Benefit by Physician at Week 4
Timepoint [4] 0 0
Week 4
Secondary outcome [5] 0 0
Physician Assessment of Cervical Dystonia Severity at Week 4
Timepoint [5] 0 0
Baseline, Week 4
Secondary outcome [6] 0 0
Physician Comparison of Benefit to Previous Injections at Week 20
Timepoint [6] 0 0
Week 20
Secondary outcome [7] 0 0
Patient Comparison of Benefit to Previous Injections at Week 20
Timepoint [7] 0 0
Week 20
Secondary outcome [8] 0 0
Patient Visual Analog Assessment of Pain at Week 4
Timepoint [8] 0 0
Baseline, Week 4
Secondary outcome [9] 0 0
Patient Assessment of Need for Retreatment at Week 4
Timepoint [9] 0 0
Baseline, Week 4

Eligibility
Key inclusion criteria
* Diagnosed with cervical dystonia/spasmodic torticollis for at least 18 months
* Successfully treated previously with botulinum toxin type A
Minimum age
18 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Breast feeding, pregnant, or could become pregnant
* Surgery or spinal cord stimulation for cervical dystonia
* Previous injections of phenol, alcohol for cervical dystonia

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/06/2007
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/06/2009
Sample size
Target
Accrual to date
Final
54
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
- Parkville
Recruitment postcode(s) [1] 0 0
- Parkville
Recruitment outside Australia
Country [1] 0 0
Argentina
State/province [1] 0 0
Buenos Aires
Country [2] 0 0
India
State/province [2] 0 0
New Delhi

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Allergan
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Medical Director
Address 0 0
Allergan
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results are available at https://clinicaltrials.gov/study/NCT00432341