Cost Effectiveness of the EndoPhys Pressure Sensing Access System vs. Radial A-line for Intra-operative Blood Pressure Monitoring

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

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-09-06

Study Completion Date

2017-04-05

Brief Summary

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This study aims to compare the time difference between radial arterial line placement and use of the EndoPhys sheath, as well as, assess the cost effectiveness of the EnoPhys sheath vs. use of a radial arterial line based on device and operating room costs.

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Detailed Description

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Conditions

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Cerebrovascular Disorders

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Caregivers

Anesthesia team will not be made aware of the purpose of the trial.

Study Groups

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EndoPhys Sheath and Radial Arterial Line

This group of patients will have both the EndoPhys sheath and the radial arterial line placed during surgery.

Group Type EXPERIMENTAL

EndoPhys Sheath and Radial Arterial Line

Intervention Type OTHER

EndoPhys Sheath

This group of patients will only receive the EndoPhys sheath during surgery.

Group Type EXPERIMENTAL

EndoPhys Sheath

Intervention Type OTHER

Interventions

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EndoPhys Sheath and Radial Arterial Line

Intervention Type OTHER

EndoPhys Sheath

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All elective neuro endovascular procedures requiring general anesthesia and continuous invasive blood pressure monitoring
* Adequate access to both the radial or femoral artery

Exclusion Criteria

* Pre-operative identification of contra-indication for radial arterial line placement
* Hemodynamic instability
* Need for continued post-operative invasive blood pressure monitoring
* Failure to obtain informed consent

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No