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Caretaker vs. Blood Pressure Monitoring With Invasive Arterial Pressure Monitoring in Patients With Septic Shock

Cooper University Health Care logo

Cooper University Health Care

Status

Active, not recruiting

Conditions

Blood Pressure

Treatments

Device: Caretaker

Study type

Observational

Funder types

Other

Identifiers

NCT03933722
18-180EX

Details and patient eligibility

About

Caretaker vs. Blood Pressure Monitoring With Invasive Arterial Pressure Monitoring in Patients With Septic Shock

Full description

The aim of this study is to compare blood pressure obtained using routine blood pressure sphygmomanometer, in patients with invasive arterial pressure monitoring that have septic shock, to a non-invasive device that continuously monitors central blood pressure (CareTaker).

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admitted with septic shock, with or without vasopressor support needed.
  • Greater than or equal to 18 years of age.
  • Have an arterial catheter already in place.

Exclusion criteria

  • No arterial catheter in place.
  • Contraindication to the application of the Caretaker device due to pre-existing finger injury.
  • Patients in whom use of a BP cuff is contraindicated.

Trial design

40 participants in 1 patient group

Caretaker
Description:
Comparing blood pressure obtained using routine blood pressure sphygmomanometer to a non-invasive device that continuously monitors central blood pressure (CareTaker).
Treatment:
Device: Caretaker

Trial contacts and locations

1

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Central trial contact

Irwin Gratz, MD

Data sourced from clinicaltrials.gov

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