Automated Non-Invasive Blood Pressure: Tracking Blood Pressure Changes Using SpO2 Data

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to design and implement methods for estimating blood pressure changes with an algorithm trained on data collected during routine patient monitoring. It uses signals from an SpO2 pulse oximeter to continuously estimate BP changes and evaluates the performance of automated rules across different clinical settings. Data will be collected to develop automated rules and to inform a larger clinical trial. The study is sponsored by GE Healthcare and conducted at Helsinki University Hospital in Finland.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Able to provide written informed consent or have a LDR to provide written informed consent;
2. Are being cared for in OR, PACU or ICU and are expected to remain in the unit for the duration of the study procedure;
3. Have an invasive blood pressure measurement as a standard of care; AND
4. Are 18 years of age or older.

Exclusion Criteria:

1. Are known to be pregnant;
2. Are breastfeeding;
3. Are suffering from infection(s) that require isolation; OR
4. Have an external heart assistant device.
5. PI or caring physician decision due to subject health condition

Where it's running

• Helsinki University Hospital
  Helsinki, Finland Recruiting
• Helsinki University Hospital
  Helsinki, Finland Not yet recruiting

Study contacts

• Study coordinator: Erika Wilkman Principal Invastigator
• Email: erika.wilkman@hus.fi
• Phone: +35894711

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.