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Completed

NCT Number: NCT01239979

Plasma Myeloperoxidase Levels in Patients With Coronary Artery Disease

The investigators sought to assess whether plasma myeloperoxidase (MPO) levels differ among patients with stable and unstable CAD patients and control subjects, and correlate with inflammatory and clinical risk factors such as ox-LDL, NO,leptin, adiponectin, sPLA2, Lp-PLA2, homocysteine and 3-nitrotyrosine in the patients.

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Key information

Age range

35 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Isfahan Cardiovascular Research Center

Isfahan, 81465-1148, Iran

About this study

Elevation of the leukocyte enzyme myeloperoxidase (MPO) in stable coronary artery disease (CAD) patients in contrast to unstable CAD patients is controversial and its relationship with some inflammatory and noninflammatory markers such as oxidized LDL (ox-LDL) and nitric oxide (NO) in the CAD patients has not been evaluated yet. Evaluation of these relationships is the aim of the study.Also the relationships between MPO and some other inflammatory biomarker such as leptin, adiponectin, sPLA2, Lp-PLA2, homocysteine and 3-nitrotyrosine are examined. This study includes 50 stable CAD, 50 unstable CAD patients and 50 controls. Plasma MPO, ox-LDL, leptin, adiponectin, sPLA2 levels are determined using enzyme immunoassay.Homocysteine and 3-nitrotyrosine are measured using HPLC-fluorescence method. Plasma total NO and other risk factors such as lipid profile, hypertension, smoking, diabetes mellitus and familial history of CAD are also determined in the patients. Results are statistically analysed and the association between all markers are assessed.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stable and unstable patients with angiographically documented coronary artery disease.
  • Control subjects without angiographically documented coronary artery disease.

All subjects Exclusion Criteria:

  • Patients with recent (with in 6 month) myocardial infarction or cardiovascular events,
  • surgery (with in 3 month),
  • cancer and
  • infective or inflammatory diseases were not included in the study.

Treatment and study plan

Primary outcomes

  1. Plasma myeloperoxidase levels

    Time frame: 3 month

Secondary outcomes

  1. Clinical risk factors

    Time frame: 3 month

Sponsors and collaborators

Lead sponsor

Isfahan University of Medical Sciences

Other

Registry information

Official study title

Evaluation of the Association Between Myeloperoxidase Levels and Cardiovascular Risk Factors in Patients With Coronary Artery Disease

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Nov 15, 2010
Registry last updated
Dec 22, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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