Status:
COMPLETED
Comparison of Intraoperative HR and RR Acquired Via ATLASense Raphael PolyMonitor and Standard Intraoperative Monitors
Lead Sponsor:
Henry Ford Health System
Conditions:
Intraoperative Monitoring
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this observational comparison study is to compare the HR and respiratory RR of intraoperative surgical patients simultaneously recorded by standard intraoperative monitors and the ATLASense...
Detailed Description
The ATLASense Raphael PolyMonitor will be placed on the patient's left chest mid sternal line in the operating room. Traditional physiologic monitors described above will also be placed on the patient...
Eligibility Criteria
Inclusion
- English speaking
- Adult males or females (above the age of 18)
- Scheduled to undergo general anesthesia during elective surgery
Exclusion
- Pregnant adult female
- Thoracic surgery
- Left lateral decubitus positioning required during procedure
- Surgery involving the left flank, or requiring surgical field involving the left flank
- Surgery involving the left chest, or requiring surgical field involving the left chest
- Allergy to adhesives
- Open wound, rash, or sore involving the left chest
- Presence of cardiac defibrillator, or pacemaker
Key Trial Info
Start Date :
October 18 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 17 2022
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT05291949
Start Date
October 18 2021
End Date
January 17 2022
Last Update
August 16 2023
Active Locations (1)
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1
Henry Ford Hospital
Detroit, Michigan, United States, 48202