- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01089972
Ultrasonographic Evaluation of the Radial and Ulnar Blood Flow After Radial Arterial Cannulation
March 31, 2011 updated by: Severance Hospital
The aim of this randomized study was to compare the impact of two different radial arterial catheters - 20G and 22G - on the changes of diameter, blood flow and velocity of radial artery and ulnar artery after induction of anesthesia and after cannulation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Seoul, Korea, Republic of
- Yonsei University College of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The patient(age >20) who are scheduled for elective surgery and need arterial
Description
Inclusion Criteria:
- The patient who are scheduled for elective surgery and need arterial cannulation
Exclusion Criteria:
- Coronary occlusive disease
- Known or suspected upper extremity peripheral arterial disease
- Coagulopathy
- DM with peripheral neuropathy
- Infection at puncture site
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
20 gauge group
|
radial artery cannulation using 20 gauge catheter
|
|
22 gauge group
|
radial artery cannulation using 22 gauge catheter
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Radial artery diameter and blood flow before and after cannulation
Time Frame: 30 min
|
30 min
|
|
Ulnar artery diameter and blood flow before and after cannulation
Time Frame: 30 min
|
30 min
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The differences of radial artery diameter and blood flow after cannulation between catheter gauge(20- and 22-G)
Time Frame: 30 min
|
30 min
|
|
The differences of ulnar artery diameter and blood flow after cannulation between catheter gauge(20- and 22-G)
Time Frame: 30 min
|
30 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2010
Primary Completion (Actual)
September 1, 2010
Study Completion (Actual)
September 1, 2010
Study Registration Dates
First Submitted
March 18, 2010
First Submitted That Met QC Criteria
March 18, 2010
First Posted (Estimate)
March 19, 2010
Study Record Updates
Last Update Posted (Estimate)
April 1, 2011
Last Update Submitted That Met QC Criteria
March 31, 2011
Last Verified
March 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- IRB 1-2009-0033
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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