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| Name | Class |
|---|---|
| Canadian Institutes of Health Research (CIHR) | OTHER_GOV |
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This study is intended to investigate the effect of cyproheptadine (a 5HT2B receptor blocker) on mitral regurgitation severity.
Ischemic mitral regurgitation (MR) is a common and morbid complication of myocardial infarction (MI), doubling heart failure and mortality with currently limited therapies. Its mechanisms have been previously linked to left ventricle (LV) remodeling with secondary deformation of otherwise normal mitral leaflets. Recent studies are introducing new mechanistic elements, allowing possibilities for potential pharmacotherapeutic approaches. Normal mitral leaflets have the capacity to enlarge and adapt to even the largest LV dilatation to prevent MR. However, this compensatory mechanism is insufficient after MI, and the leaflets are abnormally thick with fibrotic changes. Those fibrotic changes could be related to a variation in blood serotonin (5-HT) levels after MI, which has been previously reported. Serotonin is a known cause of valve fibrosis through its 5HT type 2B receptor. In sheep models, the investigators have tested the hypothesis that a 5HT type 2B receptor blocker (cyproheptadine) can prevent adverse remodeling in the valve after MI. Cyproheptadine treatment was associated with increased valve leaflet surface, attenuated leaflet thickening and collagen deposition. Importantly, treated animals had less MR compared to non-treated animals.
Thus the present study is a double-blind randomized trial to assess the effect of cyproheptadine on MR severity, mitral valve surface variation, and left ventricular size following MI. Serial imaging (3D echo and MRI) will assess valve adaptation, LV remodeling and MR.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cyproheptadine 4 Mg Oral Tablet | Experimental | Participants will receive cyproheptadine 4mg tablet orally three times a day for three months, with a daily increase of 4mg/dose if the previous dose was well tolerated, up to 0.5 mg/kg/day. |
|
| Placebo | Placebo Comparator | Participants will receive a matched placebo orally three times a day for 3 months. Daily titration similar to the treatment arm. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cyproheptadine 4 Mg Oral Tablet | Drug | Cyproheptadine treatment for 3 months |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in mitral regurgitation severity | Incidence of more than mild MR (MRI regurgitant fraction ≥ 20%) at 3 months (measured by MRI) | Baseline, 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in mitral leaflet size | Mitral leaflet size (3D echo) and its variation vs baseline (measured by echocardiography) | Baseline, 3 months |
| Change in mitral regurgitation grade | Mitral regurgitation grade (measured by echocardiography). Mitral regurgitation is graded on a scale of I-IV (grade I (mild MR), grade II (moderate MR), grade III (moderate-to-severe MR) and grade IV (severe MR)). A higher mitral regurgitation grade is generally associated with a worse outcome for the patient. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jonathan Beaudoin, MD | Contact | (418) 656-8711 | 2943 | jonathan.beaudoin@criucpq.ulaval.ca |
| Ons Marsit, PhD | Contact | (418) 656-8711 | 5773 | ons.marsit.1@ulaval.ca |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval | Recruiting | Québec | G1V 4G5 | Canada |
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| ID | Term |
|---|---|
| D009203 | Myocardial Infarction |
| ID | Term |
|---|---|
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D014652 | Vascular Diseases |
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| ID | Term |
|---|---|
| D003533 | Cyproheptadine |
| D013607 | Tablets |
| ID | Term |
|---|---|
| D003986 | Dibenzocycloheptenes |
| D001567 | Benzocycloheptenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
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| Placebo | Other | Placebo administration for 3months |
|
| Baseline, 3 months |
| Change in left ventricle size | Left ventricle size (measured by MRI ) | Baseline, 3 months |
| Change in left ventricle function | Left ventricle function (measured by MRI ) | Baseline, 3 months |
| Incidence of other valve regurgitation | Incidence of other valve regurgitation (more than mild) (measured by echocardiography) | 3 months |
| Change in mitral valve thickness | Mitral valve thickness (measured by echocardiography) | Baseline, 3 months |
| Adverse events | Composite of: Mortality, Heart failure requiring hospital admission, Mitral valve intervention (surgical/percutaneous) | 3 months and 1 year |
| Ischemic events | stroke and myocardial infarction | 3 months and 1 year |
| Bleeding events | Bleeding Academic Research Consortium (BARC) definition | 3 months and 1 year |
| Change in weight of participants | Weight gain during therapy (self-assessment by participants) | Baseline, 3 months |
| Change in the patient's perception of their health status | Self-administered questionnaire : Kansas City Cardiomyopathy Questionnaire (KCCQ). All score are represented on a 0-to-100-point scale (lower scores represent more severe symptoms and/or limitations and scores of 100 indicate no symptoms, no limitations, and excellent quality of life). | Baseline, 3 months |
| Change in the functional capacity of participants | 6-minutes walk test | 3 months, 1 year |
| Incidence of sedation | Incidence of sedation (reported by participants) | Baseline, 3 months |
| Change in depression score | Self-administered questionnaire: Patient Health Questionnaire (PHQ-9). The Patient Health Questionnaire has a scale of 0-27, with higher scores indicating a worse outcome for the patient, with more severe depression symptoms. | Baseline, 3 months |
| D007238 |
| Infarction |
| D007511 | Ischemia |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009336 | Necrosis |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011083 | Polycyclic Compounds |
| D004304 | Dosage Forms |
| D004364 | Pharmaceutical Preparations |