Heart Failure Clinical Trial
— SUCONICOfficial title:
Description and Analysis of Congestion During Hospitalization for Acute Decompensated Heart Failure
NCT number | NCT06244693 |
Other study ID # | 01-2024 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 1, 2024 |
Est. completion date | February 1, 2026 |
The goal of this observational study is to learn about the decongestion process in heart failure patients. The main question it aims to answer is: What is the behavior of congestion during hospitalization in adult patients with acute heart failure (AHF)? Participants will be evaluated in the decongestion process through clinical, analytical, and ultrasonographic variables, and they will be followed up for one year to assess mortality and rehospitalization rates in this population.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | February 1, 2026 |
Est. primary completion date | February 1, 2025 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adults diagnosed with decompensated heart failure in the emergency department or cardiology outpatient clinic at the Clinical Hospital of the University of Chile (HCUCh). - Profile of warm-wet and cold-wet type heart failure. - Spontaneous ventilation with or without non-invasive mechanical support. - Desire for participation validated through informed consent. Exclusion Criteria: - Dry-type heart failure profile (warm and cold) - Diagnostics that mimics heart failure (valvular heart disease, cardiomyopathies, and others diagnostic different from heart failure). - Septic, distributive, or obstructive shock - Polytraumatized - Severe burns - Invasive mechanical ventilation - Permanent renal replacement therapy - Severe dependence - Presence of terminal illness with a prognosis of survival less than one year - Presence of traumatic conditions that prevent the use of thoracic ultrasound, such as a flail chest or moderate to severe burn on the left hemithorax. - Lack of a support network or contact. - Cardiorespiratory arrest - Refusal to participate as indicated in the informed consent. - Presence of psychological or intellectual disability that prevents expressing the will to participate. |
Country | Name | City | State |
---|---|---|---|
Chile | Departamento Cardiovascular - Hospital Clínico Universidad de Chile | Santiago | Metropolitan |
Lead Sponsor | Collaborator |
---|---|
University of Chile |
Chile,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rehospitalization | Readmission to hospital for cardiac cause | One year from discharge | |
Primary | All cause mortality | Death from any cause | One year after discharge | |
Secondary | Cardiac death | Death form cardiac cause | One year after discharge |
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