Expired Study
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Tampa, Florida 33614


The accuracy and/or performance of the GE DINAMAP noninvasive blood pressure (NIBP) monitors may be improved with modifications in software and/or hardware monitoring techniques and/or accessories. When changes are being made to the GE Monitor, testing can be done to evaluate performance of the investigational devices during and/or after product development.


Inclusion criteria - Signed informed consent - Ability to single or dual monitor NIBP, ECG, and/or SpO2, whether or not already being monitored for any or all of these parameters. Exclusion Criteria - Any subject deemed too unstable, at the clinician's discretion, to participate in the study - Any subject with a cardiac anomaly that would cause a disparity between aortic pressures and the periphery. - Any subject who cannot tolerate, in the opinion of the clinician, multiple blood pressure measurements - Known disease state or medical condition that A) compromises circulation to the extremity (ies), B) compromises musculo-skeletal integrity, or C) otherwise contraindicates use of a NIBP cuff and/or SpO2 sensor on an extremity or ECG patches on skin - Excessive movement or excitability causing false values or no determinations (SP10 accuracy study only)



Primary Contact:

Principal Investigator
Laura Haubner, MD
University of South Florida

Backup Contact:


Location Contact:

Tampa, Florida 33614
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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