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Recruiting NCT05469165

Serotonin Receptor Blockers in Ischemic Mitral Regurgitation

Phase II Interventional Ischemic Mitral Regurgitation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cyproheptadine 4 Mg Oral Tablet, Placebo.
Who it may be relevant to
Registry conditions: Ischemic Mitral Regurgitation. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Blocking the Effects of Serotonin to Prevent Ischemic Mitral Regurgitation: a Randomized Trial (CYPRO-MR)

Overview

This study is intended to investigate the effect of cyproheptadine (a 5HT2B receptor blocker) on mitral regurgitation severity.

Detailed description

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.

Interventions

  • Drug Cyproheptadine 4 Mg Oral Tablet
    Cyproheptadine treatment for 3 months
  • Other Placebo
    Placebo administration for 3months

Primary outcome measures

  • Change in mitral regurgitation severity [Time frame: Baseline, 3 months]
Secondary outcome measures (12)
  • Change in mitral leaflet size [Time frame: Baseline, 3 months]
  • Change in mitral regurgitation grade [Time frame: Baseline, 3 months]
  • Change in left ventricle size [Time frame: Baseline, 3 months]
  • Change in left ventricle function [Time frame: Baseline, 3 months]
  • Incidence of other valve regurgitation [Time frame: 3 months]
  • Change in mitral valve thickness [Time frame: Baseline, 3 months]
  • Adverse events [Time frame: 3 months and 1 year]
  • Ischemic events [Time frame: 3 months and 1 year]
  • Bleeding events [Time frame: 3 months and 1 year]
  • Change in weight of participants [Time frame: Baseline, 3 months]
  • Change in the patient's perception of their health status [Time frame: Baseline, 3 months]
  • Change in the functional capacity of participants [Time frame: 3 months, 1 year]

Eligibility criteria

Inclusion criteria

  • Patients 18-80 years old with a 1st episode of STEMI with documented coronary obstruction.
  • Left ventricle ejection fraction (LVEF)<50% and mitral tenting area ≥ 4 cm2, OR LVEF ≤ 40% and inferior/posterior wall motion anomaly, OR LVEF≤30% and wall motion in any territory.

Exclusion criteria

  • Inability to provide informed consent
  • Hemodynamic instability / cardiogenic shock / papillary muscle rupture
  • Prior mitral valve procedure/surgery
  • Permanent atrial fibrillation (limiting imaging and MR quantification)
  • Primary mitral disease (endocarditis, rheumatic, degenerative or congenital)
  • More than mild valvular disease (other than mitral) at baseline
  • Planned cardiac surgery (CABG or valve intervention) within 3 months
  • Contraindications for MRI
  • Ongoing treatment with selective serotonin reuptake inhibitor (SSRI)
  • Chronic use of sedative medication
  • Ongoing or planned pregnancy
  • Chronic renal failure with Estimated Glomerular Filtration Rate (eGFR) < 30 mL/min
  • Neurocognitive disorder
  • Symptom or prior episode of urinary obstruction or glaucoma (relative contraindications for cyproheptadine)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Prevention

Study locations

Canada · 1 center
  • Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval — Québec

Identifiers

NCT: NCT05469165 · 22229

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗