Actively Recruiting
Gender Specific Registry in Subjects Hospitalized With Heart Failure in Santiago
Led by Fundacion de la Sociedad Chilena de Cardiologia y Cirugia Cardiovascular · Updated on 2025-08-07
500
Participants Needed
1
Research Sites
150 weeks
Total Duration
On this page
Sponsors
F
Fundacion de la Sociedad Chilena de Cardiologia y Cirugia Cardiovascular
Lead Sponsor
H
Hospital Dipreca
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is an observational registry, which main purpose is to assess sex-related differences in heart failure (HF) presentation, management, and prognosis in patients admitted to a hospital with a certain diagnosis of HF. The diagnosis will be based on European Society of Cardiology (ESC) definition of HF ( clinical syndrome characterized by symptoms and/or signs caused by a cardiac abnormality, that results in elevated intracardiac pressure and/or inadequate output at rest or exercise ). The sample will be obtained prospectively by recruitment of patients of two hospitals of Santiago de Chile.
CONDITIONS
Official Title
Gender Specific Registry in Subjects Hospitalized With Heart Failure in Santiago
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient is 18 years old or older
- Signed informed consent obtained
- Hospitalized with either:
- Acute heart failure as main cause of admission requiring cardiovascular therapy (diuretics, vasodilators, inotropes, or device), or
- Chronic heart failure diagnosed during hospitalization requiring cardiovascular therapy
You will not qualify if you...
- Present active COVID-19 infection or confirmed severe COVID-19 pneumonia
- Have a decompensated psychiatric disorder or cognitive impairment preventing survey assessment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Paola Varleta
Santiago, Santiago Metropolitan, Chile, 7700034
Actively Recruiting
Research Team
P
PAOLA VARLETA, MD
CONTACT
M
MONICA ACEVEDO, MD
CONTACT
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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