Menu
Recruiting NCT06967441

Respiratory Virus Infections in Acute Heart Failure

Observational Acute Heart Failure Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Acute Heart Failure Syndrome. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Respiratory Virus Infections in Hospitalized Patients With Acute Heart Failure Syndrome: A Prospective Multi-center Observational Study

Overview

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.

Primary outcome measures

  • Respiratory virus PCR detection rate [Time frame: Within 3 days of admission]
Secondary outcome measures (5)
  • 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: From admission to discharge during index hospitalization (upto 30 days)]
  • mortality [Time frame: 12 month]
  • Rehospitalization [Time frame: 12month]

Eligibility criteria

Inclusion criteria

  • Adult aged 19 years or older admitted to the cardiology department with acute heart failure
  • NT-proBNP >300 pg/mL
  • Clinician judgement of possible respiratory viral infection (fever >38 degrees or cough, respiratory symptoms such as sputum or consolidation on x-ray or CRP >5 mg/dL)
  • Patients who have a nasopharyngeal swab for respiratory virus PCR test performed within 72 hours of admission for any of the 3 reasons

Exclusion criteria

  • Patients with a clear other cause of acute heart failure (ex. ACS, bradycardia requiring a pacemaker, uncontrolled tachycardia, uncontrolled severe hypertension (SBP >180mmHg or DBP >110mmHg), haemoglobin <7g/dL or AHF precipitated by medication non-adherence)
  • If the cause of pulmonary oedema is prominently attributed to exacerbation of CKD
  • If there is a clear other source of infection that can explain the fever

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

South Korea · 3 centers
  • Seoul National University Bundang Hospital — Seongnam-si
  • Samsung medical center — Seoul
  • Seoul ST. Mary's Hospital — Seoul

Identifiers

NCT: NCT06967441 · SNUBH IRB NO: B-2412-941-302

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗