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Recruiting

Real-world Patient Reported Outcomes Among Patients Treated With Camzyos - CV027-1002

Mis à jour: 6 novembre, 2024   |   ClinicalTrials.gov

Impression du resumé

SONGEZ-VOUS À PARTICIPER À CET ESSAI?
Imprimez cette page et le guide pour vous aider dans vos échanges avec votre médecin.
Utilisez le guide en matière d’essai pour connaître le processus de participation à un essai clinique. Soyez au fait des principaux facteurs à considérer avant de prendre une décision et dressez la liste des questions à poser à l’équipe de soins de santé.

Détails de l’essai

  • Sexe(s)

  • 18+

    Tranche d’âge

  • 1

    Emplacement(s)

  • Recruiting

Options de traitement

Groupes de l’étude
INTERVENTION ATTRIBUÉE
Mavacamten
Drug: Mavacamten

Principaux critères d’admissibilité

Inclusion Criteria: - Participants ≥18 years of age. - Participants who are prescribed mavacamten for obstructive hypertrophic cardiomyopathy - Provided informed consent to participate in the study Exclusion Criteria: - Previously or currently enrolled in clinical trials for any cardiac myosin inhibitors - Treated for >7 days with mavacamten by the day of completing the baseline survey - Enrolled in any clinical trials at the time of or within the six-month period prior to the screening - Had heart attack requiring coronary artery bypass grafting within the three-month period prior to the screening - Had stroke or transient ischemic attack within the six-month period prior to the screening - Had moderate-to-severe lung disease which impacted the ability to perform daily activities of living and ability to breathe - Had major lung (thoracic) or heart (cardiac) surgery within the six-month period prior to the screening - Scheduled for a major surgery for the next three months, such as joint surgeries including hip replacement, abdominal surgeries, lung surgeries, heart surgeries, eye surgeries, brain surgeries, and any other major surgeries that require general anesthesia and at least an overnight hospital stay - Hospitalized requiring an overnight stay at the time of or within the two-week period prior to the screening

Nous vous recommandons fortement de contacter BMS pour signaler les effets secondaires (événements indésirables).
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici.
Signaler des effets secondaires (effets indésirables) ou des plaintes concernant la qualité du produit: Informations médicales

Des questions? Le support en direct est disponible 24/7 - Veuillez composer le 833-673-6134 ou Envoyez-nous un courriel

Des questions? Le support en direct est disponible 24/7 -
Veuillez composer le 833-673-6134 ou Envoyez-nous un courriel