Precision of IMED-4 Lung Fluid Measurements
NCT02187770
Acute Heart Failure Syndrome, Dyspnea
Boston, Massachusetts, United States
View Trial DetailsNCT Number: NCT06967441
Patients admitted to the cardiology department with acute heart failure who have a nasopharyngeal respiratory virus PCR test performed within 72 hours of admission will be enrolled in the study cohort.
The detection rate of respiratory viruses including influenza virus, RSV, and coronavirus will be analysed. The investigators will also look for seasonal changes in the frequency of respiratory viruses and differences in the clinical presentation of heart failure based on respiratory virus infection.
Interested in participating?
Request Info19 year and older
All sexes
Observational
Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, South Korea
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Within 3 days of admission
Respiratory virus PCR detection rate (especially RSV, influenza virus) in acute HF
Time frame: From admission to discharge during index hospitalization (upto 30 days)
Days of hospitalization
Time frame: From admission to discharge during index hospitalization (upto 30 days)
Rate of ICU care or ventilation
Time frame: From admission to discharge during index hospitalization (upto 30 days)
In hospital mortality
Time frame: 12 month
after discharge, 12-month mortality
Time frame: 12month
after discharge, 12-month rehospitalization
Contact information is provided by the study sponsor or research team.
Minjae Yoon
Other
Respiratory Virus Infections in Hospitalized Patients With Acute Heart Failure Syndrome: A Prospective Multi-center Observational Study
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