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

NCT ID: NCT03933722

Last Updated: 2024-02-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-02-04

Study Completion Date

2024-02-05

Brief Summary

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

Detailed Description

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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).

Conditions

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Blood Pressure

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Caretaker

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

Caretaker

Intervention Type DEVICE

Application of Caretaker device to subjects that have septic shock and that have an invasive arterial pressure monitor placed.

Interventions

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Caretaker

Application of Caretaker device to subjects that have septic shock and that have an invasive arterial pressure monitor placed.

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Cooper Health System

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Irwin Gratz, MD

Role: PRINCIPAL_INVESTIGATOR

The Cooper Health System

Locations

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Cooper University Hospital

Camden, New Jersey, United States

Site Status

Countries

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United States

Other Identifiers

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18-180EX

Identifier Type: -

Identifier Source: org_study_id

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