RECRUITINGOBSERVATIONAL
Emergency PWAS in Respiratory Infectious Disease
Emergency PanorOmic Wide Association Study in Respiratory Infectious Disease (ePWAS-RID)
About This Trial
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 presenting to emergency departments with suspected, acute, community-acquired respiratory infectious disease (scaRID). Phase 1 1. Develop an ED-ID biobank (named ePWAS-RID). Phase 2 2. Targeted research for the discovery of novel diagnostics, prognostics and therapeutics
Who May Be Eligible (Plain English)
Who May Qualify:
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
- willing to sign a consent form.
Note: scaRID is defined according to ALL three criteria:
1. Community acquired (not hospitalised for \<28 days); AND
2. 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
3. Probable respiratory infection - According to any ONE of:
1. new cough or new sputum production or
2. chest pain or
3. dyspnoea or
4. tachypnoea or
5. abnormal lung examination or
6. respiratory failure; or
7. 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.
Who Should NOT Join This Trial:
- 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 weakened immune system 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.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
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:
1. Community acquired (not hospitalised for \<28 days); AND
2. 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
3. Probable respiratory infection - According to any ONE of:
1. new cough or new sputum production or
2. chest pain or
3. dyspnoea or
4. tachypnoea or
5. abnormal lung examination or
6. respiratory failure; or
7. 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 Criteria:
* 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.
Treatments Being Tested
DIAGNOSTIC_TEST
Biomarker blood draw and saliva collection
Three peripheral 10 - 20mL blood sample (if available) Three 1 - 5mL salivary samples (if available)
Locations (1)
Hong Kong University
Hong Kong, China