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NCT05025176 Clinical Trial

Hypotension Prediction Index: Correlations Between Invasive and Non-invasive Pressure Points.

Hypotension Clinical Trial

Official title:
Hypotension Prediction Index: Correlations Between Invasive and Non-invasive Pressure Points

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05025176
Other study ID # 1791102
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 20, 2021
Est. completion date August 20, 2025

Study information
Verified date December 2023
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the clinical performance of the Hypotension Prediction Index obtained from the continuous, non-invasive Clear Sight monitor.

Description:

To evaluate the clinical performance of the Hypotension Prediction Index obtained from the continuous, non-invasive ClearSight monitor.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 50
Est. completion date August 20, 2025
Est. primary completion date August 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All Patients 18 years or older undergoing surgery with the use of general anesthesia and with planned arterial catheter placement and use of the HPI monitor. Exclusion Criteria: - Adults unable to consent - Individuals who are not yet adults ( infants, children teenagers) - Pregnant Women - Prisoners

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Non invasive arterial pressure monitoring
Non invasive arterial pressure monitoring

Locations
Country Name City State
United States UC Davis Health System Sacramento California

Sponsors (1)
Lead Sponsor Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary HPI Hypotension Prediction Index obtained from continuous, non-invasive ClearSight monitor will not differ significantly from the HPI concurrently obtained from the standard of care invasive radial arterial pressure monitor During surgical procedure
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