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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01276158
Other study ID # 200905711
Secondary ID
Status Completed
Phase N/A
First received January 11, 2011
Last updated March 9, 2017
Start date May 2011
Est. completion date December 2011

Study information

Verified date March 2017
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective randomized study was designed to compare ultrasound guided technique with Doppler assisted technique for radial arterial cannulation in infant and small children.


Description:

In infants, percutaneous cannulation of radial artery requires considerable expertise. People have been using Doppler guided radial artery cannulation technique to improve success rate for more than 20 years. Recently, Ultrasound sonography has been utilized for central line placement in pediatrics. The purpose of this study is whether ultrasound guided radial artery cannulation technique improves the success rate compared to traditional doppler guided technique.


Recruitment information / eligibility

Status Completed
Enrollment 104
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender All
Age group N/A to 48 Months
Eligibility Inclusion Criteria:

- Inclusion criteria

1. Pediatric patient undergoing scheduled major surgery which require continuous arterial pressure monitoring

2. Term neonates and children < 4 years old weighing >/= 3 kg and < 12 kg

Exclusion Criteria:

- Exclusion criteria

1. Patients with a skin wound or infection around puncture site

2. Abnormal circulation in the hand (known vascular compromise, mottling, cool skin temp relative to other hand, poor capillary refill)

3. Recent radial arterial puncture (less than 1 month)

4. Any emergency surgery or profound hemodynamic instability requiring urgent arterial cannulation.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ultrasound
Ultrasound used to place arterial line
Doppler
Doppler used to place arterial line

Locations

Country Name City State
United States University of Iowa Hospitals and Clinics Iowa City Iowa

Sponsors (1)

Lead Sponsor Collaborator
University of Iowa

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary object is to compare the first attempt success rate between each group. 10 minutes
Secondary As a secondary object, a comparison will be made between groups for overall Success rate within a 10 minute time period. 10 minutes
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