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NCT00749541 Clinical Trial

Vitamin d Levels and Coronary Catheterization

Vitamin D Deficiency Clinical Trial

Official title:
25 Hydroxy Vitamin d Levels in Patients Undergoing an Elective Coronary Catheterization

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00749541
Other study ID # vitamin d
Secondary ID
Status Completed
Phase N/A
First received September 7, 2008
Last updated December 15, 2010
Start date November 2008
Est. completion date August 2009

Study information
Verified date September 2008
Source Assaf-Harofeh Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

decreased vitamin d levels are associated with increased inflammatory markers,and renin angiotensin levels.

decreased levels were also found to be connected to increased cardiovascular mortality.

we therefore hypothesise that in patients with pathological results of coronary catheterization we will find decreased levels of 25 hydroxy vitamin d.

we will examine patients undergoing elective coronary catheterization and compare two groups: those with normal results and those with pathological results.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date August 2009
Est. primary completion date August 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:age

- >18 years,

- no known ihd

Exclusion Criteria:

- renal failure ,

- medications including vitamin d, calcium ,phosphate

- hyper or hypoparathyroidism,

- abnormal calcium or phosphate values,

- known pathological coronary catheterization.

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Assaf Harofeh Mc Zerifin

Sponsors (1)
Lead Sponsor Collaborator
Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

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