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Note: This record shows only 22 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: 19 February 2015
Main ID:  NCT00932087
Date of registration: 22/06/2009
Prospective Registration: No
Primary sponsor: Hospices Civils de Lyon
Public title: Characterization of Low Density Lipoprotein and Mechanism of the Pro Aggregant Effect Through Oxidant Stress and Lipid Exchange ECLIPSE
Scientific title: Characterization of Low Density Lipoprotein and Mechanism of the Pro Aggregant Effect Through Oxidant Stress and Lipid Exchange
Date of first enrolment: February 2009
Target sample size: 48
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00932087
Study type:  Observational
Study design:  Observational Model: Case Control, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Philippe MOULIN, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  Hospices Civils de Lyon
Key inclusion & exclusion criteria

Inclusion Criteria:

- statin and fibrate Wash out for one week

- HbA1c>7% and <12% (Arms 1 and 3)

- HbA1c<6% (Arms 2 and 4)

- Metabolic sd according NCEP III (3 out 4 criteria) (Arms 1 and 2)

Exclusion Criteria:

- secondary CV prevention



Age minimum: 30 Years
Age maximum: 75 Years
Gender: Male
Health Condition(s) or Problem(s) studied
Diabetes
Metabolic Syndrome
Intervention(s)
Procedure: Blood sample
Primary Outcome(s)
Level of plasma isoprostane and lipoperoxides [Time Frame: at baseline]
Secondary Outcome(s)
TXA2 and PF4 levels after platelet activation of control platelet exposed to LDL [Time Frame: 2 hours]
Secondary ID(s)
2008.516
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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