- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03494998
Refining and Testing the Diagnostic Accuracy of PAT-POPS
April 10, 2018 updated by: Andrew Rowland, Pennine Acute Hospitals NHS Trust
Refining and Testing the Diagnostic Accuracy of an Assessment Tool (PAT-POPS) to Predict Admission and Discharge of Children and Young People Who Attend an Emergency Department
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.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
80000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bury, United Kingdom, BL9 7TD
- Recruiting
- Fairfield General Hospital
-
Contact:
- Samah Riaz
- Phone Number: 016177882968
- Email: samah.riaz@pat.nhs.uk
-
Oldham, United Kingdom, OL1 2JH
- Recruiting
- The Royal Oldham Hospital
-
Contact:
- Samah Riaz
- Phone Number: 016177882968
- Email: samah.riaz@pat.nhs.uk
-
Rochdale, United Kingdom, OL12 2JH
- Recruiting
- Rochdale Infirmary
-
Contact:
- Samah Riaz
- Phone Number: 016177882968
- Email: samah.riaz@pat.nhs.uk
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
No older than 16 years (CHILD)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The study is designed in such a way that all patients, within the age range, will be enrolled into the study upon arrival at the Emergency Department.
Therefore, the study population will be recruited consecutively and data collection has been planned prospectively.
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Children and young people
Aged 0-16 years
|
Emergency Department-specific screening tool
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Admission or discharge
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 8, 2018
Primary Completion (Anticipated)
January 31, 2019
Study Completion (Anticipated)
January 31, 2019
Study Registration Dates
First Submitted
February 26, 2018
First Submitted That Met QC Criteria
April 10, 2018
First Posted (Actual)
April 11, 2018
Study Record Updates
Last Update Posted (Actual)
April 11, 2018
Last Update Submitted That Met QC Criteria
April 10, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 213469
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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