- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05597059
The Diagnostic Value of the First Clinical Impression of Patients Presenting to the Emergency Department (PREKEYDIA)
The Diagnostic Value of the First Clinical Impression of Patients Presenting to the Emergency Department
Finding a diagnosis for acutely ill patients places high demands on emergency medical personnel. While anamnesis and clinical examination provide initial indications and allow a tentative diagnosis, both laboratory chemistry and imaging tests are used to confirm (or exclude) the tentative diagnosis. The more precise and targeted the additional laboratory chemical or radiological diagnosis, the more quickly and economically the causal treatment of the emergency patient can be initiated.
One examination modality, which in addition to the medical history and clinical examination, could quickly provide information about the condition of the patient, their clinical picture and severity of illness, is the first clinical impression of the patient (so-called "first impression" or "end-of-bed view"). This describes the first sensory impression that the medical staff gathers from a patient. This includes visual (e.g., facial expression, gait, breathing), auditory (e.g., voice pitch, shortness of breath when speaking), and olfactory (e.g., smell of exhaled air, body odor) impressions. Clinical practice shows that a great deal of important additional information can be gathered through this first clinical impression, which, together with the history and clinical examination of the emergency patient, provides valuable clues to the underlying condition.
To date, however, only scattered data and study results exist in the medical literature on the value of the first clinical impression in the care of emergency patients. In the present prospective observational study, the study attempts to evaluate the predictive value of the first clinical impression in identifying a leading symptom and other important clinical parameters.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Upper Austria
-
Linz, Upper Austria, Austria, 4021
- Kepler University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients presenting to the emergency department between 2019-09-01 and 2020-02-28.
Exclusion Criteria:
- None.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Shortness of breath
|
Machine Learning Prediction
|
Extremity pathologies
|
Machine Learning Prediction
|
Abdominal pain
|
Machine Learning Prediction
|
Urological pathologies
|
Machine Learning Prediction
|
Chest pain
|
Machine Learning Prediction
|
Back pain
|
Machine Learning Prediction
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
AUROC for Classification of Shortness of Breath
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Shortness of Breath
|
2019-09-01 to 2020-02-28
|
AUROC for Classification of Extremity Pathologies
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Extremity Pathologies
|
2019-09-01 to 2020-02-28
|
AUROC for Classification of Abdominal Pain
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Abdominal Pain
|
2019-09-01 to 2020-02-28
|
AUROC for Classification of Urological Pathologies
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Urological Pathologies
|
2019-09-01 to 2020-02-28
|
AUROC for Classification of Chest Pain
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Chest Pain
|
2019-09-01 to 2020-02-28
|
AUROC for Classification of Back Pain
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Back Pain
|
2019-09-01 to 2020-02-28
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
AUROC for Classification of Hospital Admission
Time Frame: 2019-09-01 to 2020-02-28
|
AUROC for Classification of Hospital Admission
|
2019-09-01 to 2020-02-28
|
Confusion Matrix
Time Frame: 2019-09-01 to 2020-02-28
|
Confusion Matrix Results: true positives, true negatives, false positive, false negatives and values calculated from these results.
|
2019-09-01 to 2020-02-28
|
Descriptive Statistics
Time Frame: 2019-09-01 to 2020-02-28
|
Descriptive Statistics (e. g. age in years)
|
2019-09-01 to 2020-02-28
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PREKEYDIA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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