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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05742113
Other study ID # 10.10.2018 and 20.478.486
Secondary ID Manisa Celal Bay
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date January 1, 2021

Study information

Verified date March 2024
Source Manisa Celal Bayar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 1490
Est. completion date January 1, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 96 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Device:
Masimo Radical-7
perfusion index measuring device

Locations

Country Name City State
Turkey Manisa Celal Bayar University Manisa

Sponsors (1)

Lead Sponsor Collaborator
Manisa Celal Bayar University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perfusion index use for triage status for determination of triage status of patients with dyspnea with using perfusion index perfusion index measurement at the time of first admission to hospital
Primary Perfusion index use for triage status 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
Primary Perfusion index use for triage status 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
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