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Serotonin Receptor Blockers in Ischemic Mitral Regurgitation
RECRUITINGPhase 2Sponsored by Laval University
Actively Recruiting
PhasePhase 2
SponsorLaval University
Started2023-06-20
Est. completion2026-09
Eligibility
Age18 Years – 80 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05469165
Summary
This study is intended to investigate the effect of cyproheptadine (a 5HT2B receptor blocker) on mitral regurgitation severity.
Eligibility
Age: 18 Years – 80 YearsHealthy volunteers accepted
Inclusion Criteria: 1. Patients 18-80 years old with a 1st episode of STEMI with documented coronary obstruction. 2. 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: 1. Inability to provide informed consent 2. Hemodynamic instability / cardiogenic shock / papillary muscle rupture 3. Prior mitral valve procedure/surgery 4. Permanent atrial fibrillation (limiting imaging and MR quantification) 5. Primary mitral disease (endocarditis, rheumatic, degenerative or congenital) 6. More than mild valvular disease (other than mitral) at baseline 7. Planned cardiac surgery (CABG or valve intervention) within 3 months 8. Contraindications for MRI 9. Ongoing treatment with selective serotonin reuptake inhibitor (SSRI) 10. Chronic use of sedative medication 11. Ongoing or planned pregnancy 12. Chronic renal failure with Estimated Glomerular Filtration Rate (eGFR) \< 30 mL/min 13. Neurocognitive disorder 14. Symptom or prior episode of urinary obstruction or glaucoma (relative contraindications for cyproheptadine)
Conditions2
Heart DiseaseIschemic Mitral Regurgitation
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Actively Recruiting
PhasePhase 2
SponsorLaval University
Started2023-06-20
Est. completion2026-09
Eligibility
Age18 Years – 80 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05469165