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Completed

NCT Number: NCT00379808

Study of the Arachidonate 5-Lipoxygenase Enzyme in Affecting the Risk for Coronary Heart Disease

The purpose of this study is to determine whether a particular substance involved in inflammation, called leukotrienes, is involved in causing heart disease to occur or to progress.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Florida Family Practice Medical Group Clinic

Gainesville, Florida, 32601, United States

About this study

The focus of this study is to better understand why some adults develop heart disease and others do not. There are many known factors which play a role in causing heart disease, such as diet and lifestyle. Also, we know that inflammation, a process in the body which causes painful joints in arthritis or swelling at a site if injury, also contributes to heart disease. In particular, we will address whether leukotrienes, a component of inflammation, is involved in promoting heart disease. We will study this by giving subjects at high risk for heart disease a drug called montelukast which causes leukotrienes to have a reduced effect in the body. In addition for comparison, we will give other subjects a placebo for the same amount of time. These subjects will then be crossed-over and will receive either montelukast or placebo depending on which treatment they received first. We will compare these subjects using blood tests to see if subjects who take montelukast show signs of less inflammation caused by early heart disease as compared to subjects who do not.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

-Current hypertension (blood pressure > 140/90 mmHg) or current use of anti-hypertensive medications AND

Exclusion criteria

  • Current use of lipid-lowering medications
  • Current use of montelukast
  • Poorly controlled hypertension, where systolic blood pressure is greater than 160 or diastolic blood pressure is greater than 100
  • Use of steroid drugs, non-steroidal anti-inflammatory drugs or other anti-inflammatory medications in the two weeks prior to enrollment. (low dose aspirin ( < 325 mg) is OK, but indication must be cardiovascular)
  • Current recreational drug use
  • Other cardiovascular disease or previous cardiovascular event. These include:
  • history of angina pectoris
  • history of heart failure
  • presence of a cardiac pacemaker
  • history of myocardial infarction
  • previous revascularization procedure
  • history cerebrovascular disease including stroke and transient ischemic attack
  • Pregnancy or lactation
  • Diabetes mellitus
  • Lactose intolerance
  • Contraindications to montelukast therapy
  • Alcoholism
  • Known hepatic disease
  • Existing chronic obstructive pulmonary disease, asthma, allergic rhinitis
  • Active chronic immune, infectious, neoplastic or inflammatory diseases requiring therapy (such as active Hepatitis B, Hepatitis C, human immunodeficiency virus (HIV))
  • Immunosuppressant therapy or known immunosuppression due to disease high density lipoprotein (HDL) < 40 mg/dL (although this would be a risk factor for heart disease, because of preliminary data which indicates that montelukast may lower HDL levels, we will exclude patients with abnormally low HDL from study)
  • Other criteria at investigator discretion that are deemed to make the subject a poor candidate for the study

Treatment and study plan

Montelukast

Drug

10 mg tablet (masked by capsule) daily for 1 month

Other names: Singulair

Placebo

Drug

1 lactose-containing capsule daily for 1 month

Primary outcomes

  1. High-sensitivity C-reactive Protein

    Time frame: 1 month

    measured in a CLIA clinical laboratory facility (Quest Diagnostics, Tampa, FL)

Secondary outcomes

  1. High Density Lipoprotein (HDL)-Cholesterol

    Time frame: 1 month

    Lipid levels were determined at a clinical laboratory (Quest Diagnostics)

Other outcomes

  1. Triglycerides

    Time frame: 1 month

    measured by a clinical laboratory; Quest Laboratories

  2. Monocyte Chemotactic Protein-1 (MCP-1)

    Time frame: 1 month

    biomarker was measured by enzyme-linked immunosorbant assay (ELISA)

  3. Interleukin 1 Receptor Antagonist (IL1ra)

    Time frame: 1 month

    IL1ra was determined by enzyme-linked immunosorbant assay (ELISA)

  4. Epithelial Cell-derived Neutrophil-activating Peptide 78 (ENA-78)

    Time frame: 1 month

    biomarker determined by enzyme-linked immunosorbant assay.

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Collaborators

  • American Heart Association

Registry information

Official study title

Role of the Arachidonate 5-Lipoxygenase Pathway in Coronary Heart Disease

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Sep 22, 2006
Registry last updated
Jul 23, 2012

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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