Ultrasound Guided Versus Landmark Guided Arterial Line Placement by Emergency Medicine Interns

NCT ID: NCT03326739

Last Updated: 2020-01-22

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

2017-01-01

Study Completion Date

2019-12-31

Brief Summary

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Critically ill patients in the emergency department commonly require arterial line placement for continuous direct blood pressure monitoring, frequent arterial blood gas sampling, and frequent blood sampling. Trans-radial catheterization has been shown to reduce access site complications and increase patient comfort compared to trans-femoral access. Radial artery access on the first attempt is optimal; attempts at reentry delay care and increase the risk of vascular spasm, hematoma, infection, neurovascular injury, and pain. The traditional pulse palpation method of radial artery cannulation can be challenging, especially in patients with weak pulses (i.e. morbidly obese or hypotensive individuals).

A review of literature suggests that ultrasound guided trans-radial catheterization compared to standard pulse palpation reduces access time and increases rate of first-entry success when performed by physicians trained in ultrasound. Thus, complications ascribed to reentry are prevented and timely care is provided.

To the investigator's knowledge, only one other prospective study has been conducted to assess the utility of ultrasound guided radial artery cannulation in the emergency department. Due to the paucity of literature to support the use of ultrasound guided trans-radial catheterization in critically ill patients, the study will aim to provide further data on the topic. Both techniques are considered standard of care.

Detailed Description

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Patients presenting to the Emergency Department 18 years old or greater, who do not belong to a vulnerable group, requiring arterial line placement will be included in this trial. The investigators will randomize each patient into LM vs US. Data collected will include number of attempts, success rate, and time for procedure to be completed. PGY-1 residents will perform the arterial line placement.

Conditions

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Vascular Access Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Caregivers

Study Groups

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Ultrasound Guided A-Line Placement

Patients in this group will have ultrasound guided arterial line placement.

Group Type ACTIVE_COMPARATOR

Arterial Line Placement

Intervention Type PROCEDURE

arterial line placement

Landmark Guided A-line Placement

Patients in this group will have landmark guided arterial line placement.

Group Type ACTIVE_COMPARATOR

Arterial Line Placement

Intervention Type PROCEDURE

arterial line placement

Interventions

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Arterial Line Placement

arterial line placement

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients requiring arterial line placement.

Exclusion Criteria

* Adults Unable to Consent
* Members of Vulnerable Populations
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Temple University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ryan C Gibbons, MD

Role: PRINCIPAL_INVESTIGATOR

Lewis Katz School of Medicine at Temple University

Locations

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Lewis Katz School of Medicine at Temple University

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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24642

Identifier Type: -

Identifier Source: org_study_id

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