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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01684475
Other study ID # CJH1 Trial
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received September 11, 2012
Last updated September 12, 2012
Start date September 2012
Est. completion date September 2013

Study information

Verified date September 2012
Source Alexandra Marine and General Hospital
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the ability of CJH1 to increase the sensitivity of dopamine receptors and thereby reduce symptoms of Parkinson's Disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 21
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 85 Years
Eligibility Inclusion Criteria:

- Patient's with Parkinson's disease

Exclusion Criteria:

- Contraindications to study medication

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
CJH1 (CLR4001)


Locations

Country Name City State
Canada Gateway Rural Health Research Goderich Ontario

Sponsors (1)

Lead Sponsor Collaborator
Alexandra Marine and General Hospital

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduced signs and symptoms of Parkinson's disease Reduced signs and symptoms of Parkinson's disease 8 weeks Yes
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