ClinicalTrials.gov
ClinicalTrials.gov Menu

Ultrasonographic Evaluation of the Radial and Ulnar Blood Flow After Radial Arterial Cannulation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01089972
Recruitment Status : Completed
First Posted : March 19, 2010
Last Update Posted : April 1, 2011
Sponsor:
Information provided by:
Severance Hospital

Brief Summary:
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.

Condition or disease Intervention/treatment
Radial Artery, Regional Blood Flow Device: 22 gauge catheter Device: 20 gauge catheter

Study Type : Observational
Actual Enrollment : 80 participants
Observational Model: Case Control
Time Perspective: Prospective
Study Start Date : May 2010
Actual Primary Completion Date : September 2010
Actual Study Completion Date : September 2010

Group/Cohort Intervention/treatment
20 gauge group Device: 20 gauge catheter
radial artery cannulation using 20 gauge catheter
22 gauge group Device: 22 gauge catheter
radial artery cannulation using 22 gauge catheter



Primary Outcome Measures :
  1. Radial artery diameter and blood flow before and after cannulation [ Time Frame: 30 min ]
  2. Ulnar artery diameter and blood flow before and after cannulation [ Time Frame: 30 min ]

Secondary Outcome Measures :
  1. The differences of radial artery diameter and blood flow after cannulation between catheter gauge(20- and 22-G) [ Time Frame: 30 min ]
  2. The differences of ulnar artery diameter and blood flow after cannulation between catheter gauge(20- and 22-G) [ Time Frame: 30 min ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
The patient(age >20) who are scheduled for elective surgery and need arterial
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01089972


Locations
Korea, Republic of
Yonsei University College of Medicine
Seoul, Korea, Republic of
Sponsors and Collaborators
Severance Hospital

Responsible Party: Severance Hospital, Anesthesia and Pain Research Institute
ClinicalTrials.gov Identifier: NCT01089972     History of Changes
Other Study ID Numbers: IRB 1-2009-0033
First Posted: March 19, 2010    Key Record Dates
Last Update Posted: April 1, 2011
Last Verified: March 2010

Keywords provided by Severance Hospital:
radial artery
ulnar artery
catheterization
regional blood flow