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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03494998
Other study ID # 213469
Secondary ID
Status Recruiting
Phase
First received February 26, 2018
Last updated April 10, 2018
Start date February 8, 2018
Est. completion date January 31, 2019

Study information

Verified date April 2018
Source Pennine Acute Hospitals NHS Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Increasing attendances by children (aged 0-16 years) at UK emergency departments (EDs) is putting pressure on the National Health Service (NHS). Health professionals make complex judgements on whether children attending EDs can be sent home safely or require admission. The Pennine Acute Hospitals (PAT) Paediatric Observation Priority Score (PAT-POPS) was developed as an ED-specific screening tool for this purpose. A preliminary study showed it to be a potentially effective tool for deciding admission of children from the ED. Therefore, the focus of this study is to refine the original screening tool.


Recruitment information / eligibility

Status Recruiting
Enrollment 80000
Est. completion date January 31, 2019
Est. primary completion date January 31, 2019
Accepts healthy volunteers
Gender All
Age group N/A to 16 Years
Eligibility Inclusion Criteria:

- Children and young people aged 0-16 years of age who attend the Emergency Department

Exclusion Criteria:

- Patients who are confirmed dead on arrival at the Emergency Department

- Patients who attend the Emergency Department in cardio-respiratory arrest

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
PAT-POPS
Emergency Department-specific screening tool

Locations

Country Name City State
United Kingdom Fairfield General Hospital Bury
United Kingdom The Royal Oldham Hospital Oldham
United Kingdom Rochdale Infirmary Rochdale

Sponsors (4)

Lead Sponsor Collaborator
Pennine Acute Hospitals NHS Trust University Hospitals, Leicester, University of Manchester, University of Salford

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Admission or discharge 12 months
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