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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00271141
Other study ID # hy11/2005
Secondary ID
Status Recruiting
Phase N/A
First received December 29, 2005
Last updated December 29, 2005
Start date May 2005
Est. completion date December 2015

Study information

Verified date December 2005
Source Hillel Yaffe Medical Center
Contact Rivka Inzelberg, MD
Phone +972-4-6304607
Email inzelberg@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

The proposed work is based on the detection of a novel molecule for sensitivity to oxidative stress in humans in venous blood


Description:

Since alterations in mitochondrial functions in platelets and lymphocytes have been detected in Parkinson's disease we plan to monitor the metabolism a a new molecule (LTG) in the blood samples of Parkinson's disease patients and compare them to controls. We shall use 10 cc of venous blood and analyze serum, white blood cells and platelets. We shall not extract nor use DNA.The main purpose is to develop a marker for Parkinson's disease in venous blood.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 2015
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

Parkinson's disease Healthy control -

Exclusion Criteria:

None -

Study Design

Primary Purpose: Screening, Time Perspective: Cross-Sectional


Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (2)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center Technion, Israel Institute of Technology

Country where clinical trial is conducted

Israel, 

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