Viewing Study NCT06635018



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06635018
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-01

Brief Title: Effect of Pulse Oximeter Device on Measured Perfusion Index Values
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Pulse Oximeter Device on Measured Perfusion Index Values
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PICOMP
Brief Summary: The aim of this study is to experimentally determine the effect of pulse oximeters from different manufacturers on measured perfusion index values in healthy subjects at rest and with and without motion artifacts
Detailed Description: Perfusion index PI is one of the many vital signs monitored to assess the clinical status of a patient PI is determined from the pulsatile part of the plethysmographic curve with typical values measured on the fingers ranging from 002 to 20 Although PI is a relatively newly measured parameter it has already found application in many areas of clinical medicine It can be used as an indicator of the severity of health status in different groups of critically ill patients eg in patients with sepsis in patients after cardiac arrest for early detection of critical heart defects for indirect assessment of patient pain as an indicator of fluid therapy and reactivity or for assessment and evaluation of anaesthesia in the operating room However there is currently no standardised calculation of PI and different manufacturers use different algorithms for the calculation The consequence is that absolute measured values cannot be compared between devices

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None