Ultrasound Guided Peripheral Intravenous Catheter Insertion in the Hospitalized Patient: Long vs. Short Axis Placement

NCT ID: NCT01870661

Last Updated: 2014-06-25

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

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2013-05-31

Study Completion Date

2014-05-31

Brief Summary

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Comparison of peripheral IV catheters inserted by ultrasound using the long axis vs. the short axis technique. Our hypothesis is that long axis ultrasound placement will increase the longevity of the IV catheter.

Detailed Description

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Conditions

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Need for IV Access

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Long axis ultrasound placement of IV

Long axis ultrasound placement of IV catheter

Group Type EXPERIMENTAL

Long axis IV placement with ultrasound

Intervention Type DEVICE

Peripheral IV placement with the ultrasound probe viewing the vessel in the long axis.

Short axis ultrasound placement of IV

Long axis ultrasound placement of IV catheter

Group Type ACTIVE_COMPARATOR

Short axis IV placement with ultrasound

Intervention Type DEVICE

Peripheral IV placement with the ultrasound probe viewing the vessel in the short axis.

Interventions

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Long axis IV placement with ultrasound

Peripheral IV placement with the ultrasound probe viewing the vessel in the long axis.

Intervention Type DEVICE

Short axis IV placement with ultrasound

Peripheral IV placement with the ultrasound probe viewing the vessel in the short axis.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* A patient who needs PIV access for intravenous medications and resuscitation either on a medical-surgical floor or in the ICU
* After floor team (including RN and/or house staff) and IV Nurse have attempted and failed or is not available

Exclusion Criteria

* Need for vasopressors
* Need for TPN
* Need for hemodynamic monitoring
* Non English speaking patient
* Patients who are unable to consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Beth Israel Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Michael Silverberg, MD

Role: PRINCIPAL_INVESTIGATOR

Beth Israel Medical Center

Locations

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Beth Isreal Medical Center

New York, New York, United States

Site Status

Countries

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United States

Other Identifiers

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035-13

Identifier Type: -

Identifier Source: org_study_id

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