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| ID | Type | Description | Link |
|---|---|---|---|
| AHA0615253B | Other Grant/Funding Number | American Heart Associatino |
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| Name | Class |
|---|---|
| American Heart Association | OTHER |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | 1 lactose-containing capsule daily for 1 month |
|
| Montelukast 10 mg | Active Comparator | 1 montelukast 10 mg tablet (masked by capsule) daily for 1 month |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| montelukast | Drug | 10 mg tablet (masked by capsule) daily for 1 month |
|
| Measure | Description | Time Frame |
|---|---|---|
| High-sensitivity C-reactive Protein | measured in a CLIA clinical laboratory facility (Quest Diagnostics, Tampa, FL) | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| High Density Lipoprotein (HDL)-Cholesterol | Lipid levels were determined at a clinical laboratory (Quest Diagnostics) | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| Triglycerides | measured by a clinical laboratory; Quest Laboratories | 1 month |
| Monocyte Chemotactic Protein-1 (MCP-1) | biomarker was measured by enzyme-linked immunosorbant assay (ELISA) |
Inclusion Criteria:
-Current hypertension (blood pressure > 140/90 mmHg) or current use of anti-hypertensive medications AND
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Julie A Johnson, PharmD | University of Florida | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Florida Family Practice Medical Group Clinic | Gainesville | Florida | 32601 | United States |
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Patients were recruited based on flyers posted in public places, through recontact of patients in previous studies, and patients cared for in a family medicine clinic
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| ID | Title | Description |
|---|---|---|
| FG000 | Placebo Then Montelukast | Patients were randomized in a crossover design to placebo or montelukast. Patients int this randomization arm received 4 weeks of placebo then 4 weeks of montelukast. There was no washout between crossover |
| FG001 | Montelukast Then Placebo | Patients were randomized in a crossover design to placebo or montelukast. Patients in this arm got montelukast for 4 weeks and then placebo for 4 weeks. There was no washout period |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Intervention Period 1 (4 Weeks) |
| |||||||||||||
| Intervention Period 2 (4 Weeks) |
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| ID | Title | Description |
|---|---|---|
| BG000 | All Participants | Patients were randomized in a crossover design, but baseline characteristics were presented for all participants. Likewise data are not separated by order of treatment because there were no order effects |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | High-sensitivity C-reactive Protein | measured in a CLIA clinical laboratory facility (Quest Diagnostics, Tampa, FL) | based on patients who completed the entire study | Posted | Median | Inter-Quartile Range | mg/dl | 1 month |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Placebo | This is all participants who received placebo, whether in first or second intervention |
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Because there were no order effects, the placebo groups were combined and the montelukast groups were combined. Therefore results from each of these are not reported by arm.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr Julie Johnson, PI | University of Florida | 352-273-6007 | johnson@cop.ufl.edu |
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| ID | Term |
|---|---|
| D003327 | Coronary Disease |
| D007249 | Inflammation |
| ID | Term |
|---|---|
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D014652 | Vascular Diseases |
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| ID | Term |
|---|---|
| C093875 | montelukast |
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| Placebo | Drug | 1 lactose-containing capsule daily for 1 month |
|
| 1 month |
| Interleukin 1 Receptor Antagonist (IL1ra) | IL1ra was determined by enzyme-linked immunosorbant assay (ELISA) | 1 month |
| Epithelial Cell-derived Neutrophil-activating Peptide 78 (ENA-78) | biomarker determined by enzyme-linked immunosorbant assay. | 1 month |
| NOT COMPLETED |
|
|
| Participants |
|
| Age Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
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| Units | Counts |
|---|
| Participants |
|
|
|
| Secondary | High Density Lipoprotein (HDL)-Cholesterol | Lipid levels were determined at a clinical laboratory (Quest Diagnostics) | those completing entire study | Posted | Median | Inter-Quartile Range | mg/dl | 1 month |
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|
|
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| Other Pre-specified | Triglycerides | measured by a clinical laboratory; Quest Laboratories | those completing the entire study | Posted | Median | Inter-Quartile Range | mg/dl | 1 month |
|
|
|
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| Other Pre-specified | Monocyte Chemotactic Protein-1 (MCP-1) | biomarker was measured by enzyme-linked immunosorbant assay (ELISA) | those who completed the entire study | Posted | Median | Inter-Quartile Range | pg/ml | 1 month |
|
|
|
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| Other Pre-specified | Interleukin 1 Receptor Antagonist (IL1ra) | IL1ra was determined by enzyme-linked immunosorbant assay (ELISA) | all participants who completed the entire study | Posted | Median | Inter-Quartile Range | pg/ml | 1 month |
|
|
|
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| Other Pre-specified | Epithelial Cell-derived Neutrophil-activating Peptide 78 (ENA-78) | biomarker determined by enzyme-linked immunosorbant assay. | those completing the entire study | Posted | Median | Inter-Quartile Range | pg/ml | 1 month |
|
|
|
|
| 0 |
| 21 |
| 0 |
| 21 |
| EG001 | Montelukast | This is all patients who received montelukast, whether in the first or second intervention period | 0 | 22 | 0 | 22 |
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| D010335 |
| Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |