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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03391128
Other study ID # P3NPhemodialysis
Secondary ID
Status Completed
Phase N/A
First received December 28, 2017
Last updated January 4, 2018
Start date January 1, 2005
Est. completion date January 31, 2005

Study information

Verified date January 2018
Source Toujinkai Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates whether circulating levels of aminoterminal propeptide of type III procollagen (PIIINP) can predict the cardiovascular events in hemodialysis patients.


Description:

Type III collagen abundantly exists in the cardiovascular system including the aorta and heart. The aminoterminal propeptide of type III procollagen (PIIINP) is an extension peptide of type III procollagen, which is cleaved off stoichiometrically during conversion from type III procollagen to type III collagen and liberated to serum. Elevated serum concentrations of PIIINP are considered a marker of higher collagen turnover and tissue fibrosis including the heart and vascular system. In this study, the investigators prospectively examined whether serum levels of PIIINP could be a biomarker for predicting cardiovascular events in hemodialysis patients.


Recruitment information / eligibility

Status Completed
Enrollment 244
Est. completion date January 31, 2005
Est. primary completion date January 31, 2005
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- End-stage kidney disease patients who had been undergoing maintenance hemodialysis over one year in Toujinkai Hospital at the point of January 1, 2005

Exclusion Criteria:

- Histories of coronary events and/or interventions

- Congestive heart failure of New York Heart Association grades III to IV

- Moderate or worse valvular heart disease

- Permanent pacemaker implantation

- Idiopathic cardiomyopathy

- Chronic obstructive pulmonary disease

- Malignancy

- Acute hepatitis, chronic hepatitis, or liver cirrhosis including carrier of hepatitis virus

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Japan Toujinkai Hospital Kyoto

Sponsors (1)

Lead Sponsor Collaborator
Toujinkai Hospital

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiovascular events Cardiac deaths, non-fatal acute myocardial infarction, obstructive coronary artery disease needing intervention, vasospastic angina identified by angiography, heart failure needing hospitalization, bradycardia needing pacemaker implantation, dissecting aortic aneurysm, cardiac valvular disease needing valve replacement, peripheral artery disease needing bypass surgery or leg amputation. January 1, 2005 to January 31, 2011
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