NCT01276171

Brief Summary

Radial arterial cannulation is a common invasive procedure for real-time measurement of arterial blood pressure. Placement of the arterial catheter using conventional palpation is often relatively easy and quick, but this is not always true. A relatively new method for direct visualization of the artery is the use of two-dimensional ultrasound. This technique allows cannulation of the artery to take place under real-time visualization and may increase the success rate of first time pass of the needle. Another technique utilizing Doppler has also proven to be effective in cannulating the radial artery. This technique utilizes changes in acoustic pitch as the probe passes directly over the artery. The primary objective of this study is to compare the first attempt success rate for radial artery cannulation among the palpation, Doppler and U/S guided technique when applied by trainees. Secondary outcomes include: success rate within 5 minutes, successful, number of attempts required, and correlation between success rate and operator experience for successful cannulation of the radial artery.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
749

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2010

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2010

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

January 11, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 13, 2011

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
3.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2015

Completed
2.2 years until next milestone

Results Posted

Study results publicly available

June 26, 2017

Completed
Last Updated

June 26, 2017

Status Verified

April 1, 2017

Enrollment Period

1.8 years

First QC Date

January 11, 2011

Results QC Date

January 12, 2017

Last Update Submit

April 10, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • First Attempt Success Rate With 3 Different Technique

    The primary objective of this study is to compare the first attempt success rate for radial artery cannulation between the palpation, Doppler and U/S guided technique when applied by anesthesia trainees. Secondary outcomes include: success rate within 5 minutes, time to successful cannulation compared with three different techniques.

    5 minutes

Secondary Outcomes (2)

  • Time to Successful Cannulation

    5 minutes

  • Total Success Rate

    5 min

Study Arms (3)

Ultrasound

ACTIVE COMPARATOR

Participants will place arterial line using ultrasound technique

Procedure: Ultrasound

Doppler

ACTIVE COMPARATOR

Participants will place arterial line using doppler technique

Procedure: Doppler

Palpation

ACTIVE COMPARATOR

Participants will place arterial line using palpation technique

Procedure: Palpation

Interventions

UltrasoundPROCEDURE

Participants will place arterial line using ultrasound technique

Ultrasound
DopplerPROCEDURE

Participants will place arterial line using doppler technique

Doppler
PalpationPROCEDURE

Participants will place arterial line using Palpation technique

Palpation

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Main OR patients at UIHC who require arterial catheter placement for surgery

You may not qualify if:

  • The patients who will be excluded from the study include those who have had arterial cannulation in the previous month, infections at site of insertion, and AV shunts in upper extremity.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Iowa Hospitals and Clinics

Iowa City, Iowa, 52242, United States

Location

MeSH Terms

Interventions

High-Energy Shock Waves

Intervention Hierarchy (Ancestors)

Ultrasonic WavesSoundRadiation, NonionizingRadiationPhysical Phenomena

Results Point of Contact

Title
Dr. Kenichi Ueda
Organization
University of Iowa Hospitals and Clinics

Study Officials

  • Kenichi Ueda, MD

    University of Iowa

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Associate Professor

Study Record Dates

First Submitted

January 11, 2011

First Posted

January 13, 2011

Study Start

February 1, 2010

Primary Completion

December 1, 2011

Study Completion

April 1, 2015

Last Updated

June 26, 2017

Results First Posted

June 26, 2017

Record last verified: 2017-04

Data Sharing

IPD Sharing
Will not share

We are not planning on sharing IPD.

Locations