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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00365911
Other study ID # 2006/038
Secondary ID
Status Completed
Phase N/A
First received August 17, 2006
Last updated June 1, 2011
Start date March 2006
Est. completion date December 2009

Study information

Verified date June 2011
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Blood sample is taken for measurement of serum creatinine, cystatin C, clone V haemoglobin, cholesterol, urine acid, glycemia and CRP.

The medical file is gathered. There will be searched for an association between renal function and cardiovascular risk factors and risk factors by exposition to toxic substantia during work.


Recruitment information / eligibility

Status Completed
Enrollment 2000
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- 20-55 years

- Male and female subjects

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Taking blood sample
A blood sample will be taken.

Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Ghent Medical Laboratory CRI, Prevemed-Medibo

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary A possible association between renal clearance and found cardiovascular risk factors and risk factors by exposition to toxic substantia during work. At time T0 No
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