- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05742113
Emergency Classification According to Fingertip Circulation
DYSPNEA: PERFUSION INDEX and TRIAGE STATUS (the Name of the Project)
Dyspnea is one of the most common reasons for admission to the emergency department[1]. Oxygen saturation has great importance in determining the triage status of patients admitted to the hospital with dyspnea and planning the emergency treatment [2].
Peripheral perfusion index (PI), which shows tissue oxygenation is a noninvasive way of demonstrating tissue perfusion in critically ill patients. Studies have shown that PI is an accurate, fast and reliable pulse oximetry-based indicator of tissue perfusion [3-5]. PI shows the perfusion status of the tissue in the applied area for an instant and a certain time interval. The PI value ranges from 0.02% (very weak) to 20% (strong) [6].
Triage scales are used to distinguish emergency and non-emergency patients. The emergency triage system is used to quickly determine the care priorities of patients during admission to the emergency department[7,8].
It is important to make the triage classification for dyspnea in emergency services quickly and accurately to start the treatment protocols as early as. In this study, the investigators aimed to determine the relationship between perfusion index and the emergency triage classification in patients admitted to the emergency department with dyspnea.
Study Overview
Detailed Description
Purpose: To determine the effect of PI measurement on the emergency triage classification in patients with dyspnea.
Methods: Adult patients who presented with dyspnea and whose perfusion index values were measured with Masimo Radical-7 device at the time of admission, at the first hour and the second hour of admission were included in the study. The PI and oxygen saturation measured by finger probes were compared and the superiority of their effects on the emergency triage classification was compared.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Manisa, Turkey, 45030
- Manisa Celal Bayar University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adult patients over the age of 18 who presented with dyspnea
- whose perfusion index values were measured at the time of first admission (arrival time), at the first hour and the second hour of admission were included in the study
Exclusion Criteria:
- Patients who applied due to the mechanism of trauma,
- patients with known vascular disease (Buerger's disease, peripheral artery disease, etc.), -patients with COVID-19 PCR positivity
- whose perfusion index measurement could not be completed due to hospitalization or discharge were excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Triage status red
the relationship between the perfusion index and the emergency triage classification in patients admitted to the emergency department with dyspnea.
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perfusion index measuring device
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perfusion index use for triage status
Time Frame: perfusion index measurement at the time of first admission to hospital
|
for determination of triage status of patients with dyspnea with using perfusion index
|
perfusion index measurement at the time of first admission to hospital
|
|
Perfusion index use for triage status
Time Frame: perfusion index measurement at the time of the first hour after admission to hospital
|
for determination of triage status of patients with dyspnea with using perfusion index
|
perfusion index measurement at the time of the first hour after admission to hospital
|
|
Perfusion index use for triage status
Time Frame: perfusion index measurement at the time of the second hour after admission to hospital
|
for determination of triage status of patients with dyspnea with using perfusion index
|
perfusion index measurement at the time of the second hour after admission to hospital
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Cumhur M TULAY, Ass.Prof., Ass.Prof.
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10.10.2018 and 20.478.486
- Manisa Celal Bayar University (Other Identifier: 2018-213)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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