Effect of Genetic Polymorphism on the Clinical Outcome of Patients With Heart Failure
NCT03122834 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 246
Last updated 2025-02-20
Summary
Heart failure (HF) is one the most common cause of hospitalization and represents the end stage of a variety of heart conditions; it is associated with significant morbidity and mortality.The pathophysiology of HF is centered on increased activity in the adrenergic and renin-angiotensin-aldosterone systems (RAAS), which leads to vasoconstriction and fluid restriction with further deleterious effect on cardiac function. Β-blockers, angiotensin converting enzyme inhibitors (ACEIs)/angiotensin II receptor blockers (ARBs) and aldosterone antagonists reduce activity in these pathways and have shown prognostic benefit, thus are the foundation of HF therapy.There is a growing body of evidence that variation in proteins within the sympathetic axis and RAAS influence drug response thus increasingly pharmacogenetics of HF research is being sought as a way to optimize HF treatment and advance new drug development in this area.
Conditions
Sponsors & Collaborators
-
Misr International University
collaborator OTHER -
National Heart Institute
collaborator UNKNOWN -
Ain Shams University
lead OTHER
Principal Investigators
-
Neven M. Sarhan, PhD · Misr International University
-
Mona F. Schaalan, PhD · Misr International University
-
Bassem Zarif, MD · National Heart Institute
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-04-15
- Primary Completion
- 2024-04-10
- Completion
- 2024-06-14
Countries
- Egypt
Study Locations
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