Observational Study Evaluating Long-term Health Outcomes of Canadian DUODOPA-treated Patients

Study Identifier
P14-506
CT.gov Identifier
NCT02485600
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Scientific Result Summary
Available Language(s): English
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Study Details

Medical Condition
  • Parkinson's Disease
    • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    18 - 99 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Diagnosed with advanced Parkinson's Disease * Prescribed Duodopa by his/her treating physician.
    Exclusion Criteria:
    * Patients who were previously treated with Duodopa. * Presence of other condition that, in the opinion of the treating physician, prohibits the patient from participating in the study or obscures the assessment of the treatment of advanced PD.

    Protocol Summary

    This is an open-label, postmarketing, observational study to document health outcomes, in Canadian patients with advanced Parkinson's disease and long-term treatment with Duodopa (levodopa/carbidopa intestinal gel).

    Study Locations

    Location
    Status
    Location
    University of Calgary /ID# 151948
    Calgary, Alberta, Canada, T2N 4Z6
    Status
    Not applicable
    Location
    Zeidler Ledcor Centre /ID# 135979
    Edmonton, Alberta, Canada, T6G 2X8
    Status
    Not applicable
    Location
    St. Boniface Clinic, CA /ID# 162092
    Winnipeg, Manitoba, Canada, R2H 2A5
    Status
    Not applicable
    Location
    Hamilton Health Sciences /ID# 148808
    Hamilton, Ontario, Canada, L8L 2X2
    Status
    Not applicable
    Location
    Kingston General Hospital /ID# 144942
    Kingston, Ontario, Canada, K7L 2V7
    Status
    Not applicable
    Location
    London Health Sciences Centre /ID# 138434
    London, Ontario, Canada, N6A 5A5
    Status
    Not applicable
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