Philips Advanced Monitoring Cuff (i.e. AMC)
DeviceInvestigational, non-invasive upper arm cuff
NCT Number: NCT06895590
The purpose of this study is to compare measurements of blood pressure (BP) and fluid responsiveness between the Philips AMC and invasive radial arterial line in surgical patients.
Interested in participating?
Request Info18 year and older
All sexes
Observational
LMU Klinikum , Campus Großhadern, München, Bavaria, Germany
Primary Objective:
Secondary Objectives:
Hypothesis: Blood pressure measurements derived from the Philips AMC are equivalent to the radial arterial line and superior to the oscillometric non-invasive blood pressure (NIBP) cuff.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The following stratification criteria must be met across the study sites and hence targeted enrollment may be required:
Exclusion criteria
Investigational, non-invasive upper arm cuff
Time frame: Approximately 8 months accrual and follow-up evaluation period.
The comparison of systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial pressure (MAP) between the Philips AMC and radial arterial line.
Contact information is provided by the study sponsor or research team.
Philips Clinical & Medical Affairs Global
Industry
Acronym: HIPULSE
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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