Status:

RECRUITING

Emergency PWAS in Respiratory Infectious Disease

Lead Sponsor:

The University of Hong Kong

Conditions:

Viral Infections

Bacterial Infections

Eligibility:

All Genders

18-100 years

Brief Summary

Develop an emergency PanorOmics Wide Association Study (ePWAS) for the early, rapid biological and pathophysiological characterisation of known and novel Infectious Diseases in adult patients presenti...

Detailed Description

Introduction Pandemic Preparedness The COVID-19 pandemic has affected over 220 million people, claimed over 450 000 lives and invoked variable responses across the world. Delays in acquiring quality...

Eligibility Criteria

Inclusion

  • Patients eligible for enrolment include:
  • With reference to previous inclusion criteria are:
  • Adults ≥18 years of age; AND
  • Suspected, acute, community-acquired, respiratory, infectious disease (scaRID)\*; AND
  • Informed consent.
  • Note: scaRID is defined according to ALL three criteria:
  • Community acquired (not hospitalised for \<28 days); AND
  • Acute infection (defined as symptom onset \<8 days and any ONE of reported fever or chills or aural temperature \>37.5°C or hypothermia or leucocytosis or leucopaenia or new altered mental status); AND
  • Probable respiratory infection - According to any ONE of:
  • new cough or new sputum production or
  • chest pain or
  • dyspnoea or
  • tachypnoea or
  • abnormal lung examination or
  • respiratory failure; or
  • physician's judgment (presenting with systemic or gastrointestinal symptoms).
  • Control subjects will be drawn from two groups:
  • The worried well - adult patients with a National Early Warning Score (NEWS) \<3 and a temperature \<37.5°C.
  • Relatives or accompanying friends with no acute illness.

Exclusion

  • Refusal of consent;
  • Recent hospitalisation (\<28 days);
  • Enrolled in another clinical trial
  • Cellulitis;
  • Skin or orthopaedic infections;
  • Urinary tract infection;
  • Acute abdominal sepsis;
  • Sexual transmitted disease;
  • Human immunodeficiency virus (HIV) infection;
  • Immunocompromised/potential neutropenic fever;
  • Solid organ or haematopoietic stem-cell transplant within the previous 90 days;
  • Active graft-versus-host disease or bronchiolitis obliterans;
  • Severe traveller's disease requiring urgent hospitalisation and management including malaria, dengue, typhoid and other rickettsial diseases;
  • Stroke;
  • Toxidrome;
  • Non-organic acute psychosis.

Key Trial Info

Start Date :

April 11 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

May 1 2025

Estimated Enrollment :

2000 Patients enrolled

Trial Details

Trial ID

NCT05336851

Start Date

April 11 2023

End Date

May 1 2025

Last Update

May 23 2024

Active Locations (1)

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Hong Kong University

Hong Kong, China