World Health Organization site
Skip Navigation Links

Main
Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00932581
Date of registration: 01/07/2009
Primary sponsor: Teva Pharmaceutical Industries
Public title: Bradykinesia Subscale Administered Alone Versus Regular Administration: Psychometric Properties Bravura
Scientific title: Investigation of the Psychometric Properties of the Bradykinesia Subscale When Administered Alone Versus as a Component of the Entire Motor Examination Section of the Unified Parkinson's Disease Rating Scale
Date of first enrolment: June 2009
Target sample size: 110
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00932581
Study type:  Observational
Study design:  Observational Model: Case Control, Time Perspective: Prospective  
Countries of recruitment
United States
Contacts
Name:   Philip Buck, PhD, MPH
Address: 
Telephone:
Email:
Affiliation:  Teva Neuroscience, Inc.
Key inclusion & exclusion criteria

Inclusion Criteria:

1. Male or Female at least 30 years of age

2. Willing to be assessed using the motor examination section of the UPDRS and the
SPES/SCOPA motor evaluation

3. Patients must be willing and able to give written informed consent prior to
performing an study procedures

4. Be in the "ON" State (only for patients who fluctuate between "ON" and "OFF" states)

Exclusion Criteria:

1. Absence of bradykinesia at the time of assessment

2. Hoehn and Yahr stage not available from patient's chart or not assessed between 3 and
180 days prior to clinic visit

3. Has received and experimental drug within the last thirty (30) days



Age minimum: 30 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Parkinson's Disease
Intervention(s)
Other: Bradykinesia subscale of UPDRS Motor Examination
Other: Bradykinesia UPDRS Motor Full Examination
Primary Outcome(s)
Scores on the UPDRS motor evaluation subscale are equivalent. [Time Frame: 4 months]
Secondary Outcome(s)
Correlations between the UPDRS motor examination bradykinesis subscale and the remaining UPDRS motor examination items, Hoeh and Yahr stage, Schwab and England scale, and SPES/SCOPA motor evaluation. [Time Frame: 4 months]
Secondary ID(s)
PM105
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.1 - Version history