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NCT00309426 Clinical Trial

Effect of Fetuin A in Hemodialysis Patients

Malnutrition Clinical Trial

Official title:
The Effect of Serum Fetuin A Concentration on the 5-Year Prognosis in Hemodialysis Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00309426
Other study ID # CT2006003
Secondary ID
Status Active, not recruiting
Phase N/A
First received March 27, 2006
Last updated May 18, 2006
Start date March 2001
Est. completion date March 2006

Study information
Verified date March 2006
Source University of Shizuoka
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Observational

Clinical Trial Summary

The purpose of this study is to examined the effect of fetuin A on atherosclerosis and prognosis in hemodialysis patients.

Description:

Fetuin A is known to be a potent inhibitor of ectopic calcification in plasma, and the concentration of fetuin A is closely associated with protein nutritional status. The purpose of this study is to examine whether the plasma concentration of fetuin A is associated with atherosclerosis and 5-year prognosis in hemodialysis patients.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 300
Est. completion date March 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A to 70 Years
Eligibility Inclusion Criteria:

- Hemodialysis for at least 6 months

Exclusion Criteria:

- Disabled patients

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Locations
Country Name City State
Japan Maruyama Hospital Hamamatsu Shizuoka

Sponsors (2)
Lead Sponsor Collaborator
University of Shizuoka Maruyama Memorial General Hospital

Country where clinical trial is conducted

Japan, 

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