Actively Recruiting

All Genders
Healthy Volunteers
ID05884892

Egyptian Hypertrophic Cardiomyopathy Program

Led by Magdi Yacoub Heart Foundation · Updated on 2023-06-01

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting the Egyptian Hypertrophic Cardiomyopathy (HCM) Program to understand the incidence, severity, and characteristics of HCM in Egypt. The study also aims to explore genetic factors and the underlying molecular and cellular mechanisms that influence the disease's different forms. A key focus is on patients who have genetic markers but no symptoms, which may provide insight into how the disease develops. The program involves detailed characterization of patients and their relatives through clinical, genetic, and laboratory assessments. It includes training for Egyptian medical professionals in advanced diagnostic and treatment techniques. The study uses state-of-the-art medical, surgical, and interventional methods tailored to each patient's condition, with ongoing collection and analysis of human tissue samples from surgical procedures. Participants will undergo regular follow-ups approximately once per year, over an average of five years, to monitor disease progression and severity through clinical exams, imaging, and genetic testing. The study measures include the incidence of HCM, clinical severity, cardiac phenotype, and genotype correlations. This long-term observation aims to improve understanding and management of HCM in Egypt while supporting advanced training and research development.

CONDITIONS

Brief Title

Egyptian Hypertrophic Cardiomyopathy Program

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with hypertrophic cardiomyopathy who are willing and consent to participate.
  • Family members of these patients who are willing and consent to participate.
Not Eligible

You will not qualify if you...

  • Refusal to consent to participate in the registry program.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 5 years

Participants are observed over time to define the incidence, severity, phenotype, and genotype of hypertrophic cardiomyopathy, as well as to study disease mechanisms.

Approximately 5 visits, about 1 visit per year

Trial Site Locations

Total: 1 location

1

Aswan Heart Centre - Magdi Yacoub Heart Foundation

Aswān, Egypt

Actively Recruiting

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Research Team

M

Magdi H Yacoub, FRS OM

S

Shehab M Anwer, MBBCh., MRes

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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