Ultrasonography For Radial Artery Diameter Measurement And Its Correlation With Allen Test

Sponsor
Istanbul University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03405428
Collaborator
(none)
500
1
1
2.9
172.9

Study Details

Study Description

Brief Summary

In this study, the investigators will investigate how patients' radial artery diameters change according to sex, age, height, weight and body mass index by measuring radial artery diameter using ultrasonography. The correlation of Allen test with doppler ultrasonography will also be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Other: Allen test
  • Other: Radial artery diameter measurement by ultrasonography
  • Other: Ulnar artery doppler ultrasonography
N/A

Detailed Description

Arterial catheterization for continuous hemodynamic monitoring or frequent blood sampling is a common procedure in anesthesia and critical care setting. The most commonly used site for arterial catheterization is the radial artery because of its superficial course, alternate blood supply to hand via ulnar artery and a low rate of complications. Allen test is a simple, but not reliable, method for assessing the safety of radial artery catheterization. Intraarterial catheterization has some complications such as hematoma, vasospasm, arterial thrombosis, necrosis of skin overlying. Using larger size cannula from radial artery diameter, increase rate of complications. The purpose of this study is to investigate the corelation of radial artery diameter with sex, age, height, weight and body mass index for determination of proper cannula size and investigation of correlation between Allen test and doppler ultrasonography.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Radial Artery Diameter Measurement By Ultrasonography For Determination Of Proper Cannula Size And Investigation Of Correlation Between Allen Test And Doppler Ultrasonography
Actual Study Start Date :
Feb 1, 2018
Anticipated Primary Completion Date :
Apr 1, 2018
Anticipated Study Completion Date :
Apr 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Other: All patients

Other: Allen test
Before induction, with firm occlusive pressure held on both the radial and ulnar arteries, the patient is asked to clench his or her fist several times until the palmar skin is blanched. The patient is then instructed to unclench the fist, and then ulnar artery pressure is released while maintaining occlusion of the radial artery. Overextension of the hand and wide spreading of the fingers should be avoided because it can lead to falsely abnormal results. The time required for palmar capillary refill is noted. An abnormal Allen test result was defined as a recovery time of more than 10 seconds.

Other: Radial artery diameter measurement by ultrasonography
Ultrasonography measurements will be performed with a linear probe before and after induction. The non-dominant hand of the patient will be fixed in the anatomical position on the arm chair. The wrist joint of patient will be extended to 30 degrees with a wrist pad. The USG probe will be transversally placed 2 cm proximal to the styloid process and the short axes of the radial artery will be scanned. The diameter of the radial artery will be measured and recorded.

Other: Ulnar artery doppler ultrasonography
Ultrasonography measurements will be performed with a linear probe before and after induction. The non-dominant hand of the patient will be fixed in the anatomical position on the arm chair. The wrist joint of patient will be extended to 30 degrees with a wrist pad. The USG probe will be transversally placed 2 cm proximal to the styloid process and the short axes of the ulnar arter will be scanned. The blood fow of ulnar artery will be measured and recorded.

Outcome Measures

Primary Outcome Measures

  1. change of the radial artery diameter according to sex, age, height, weight and body mass index [5 minutes prior to anesthesia induction]

    Ultrasonography measurements will be performed with a linear probe. The non-dominant hand of the patient will be fixed in the anatomical position on the arm chair. The wrist joint of patient will be extended to 30 degree with a wrist pad. The Ultrasonography probe will be transversally placed 2 cm proximal to the styloid process and the short axes of the radial artery will be scanned. The diameter of the radial artery will be measured and recorded.

Secondary Outcome Measures

  1. correlation between Allen test and doppler ultrasonography. [5 minutes prior to anesthesia induction]

    Before induction, with firm occlusive pressure held on both the radial and ulnar arteries, the patient is asked to clench his or her fist several seconds until the palmar skin is blanched. The patient is then instructed to unclench the fist, and then ulnar artery pressure is released while maintaining occlusion of the radial artery. The time required for palmar capillary refill is noted. An abnormal Allen test result was defined as a recovery time of more than 10 seconds. Ultrasonography measurements will be performed with a linear probe. The non-dominant hand of the patient will be fixed in the anatomical position on the arm chair. The wrist joint of patient will be extended to 30 degree with a wrist pad. The USG probe will be transversally placed 2 cm proximal to the styloid process and the short axes of the ulnar artery will be scanned. The blood fow of ulnar artery will be measured and recorded.

  2. change of the radial artery diameter according to sex, age, height, weight and body mass index after the induction [5 minutes following to anesthesia induction]

    Ultrasonography measurements will be performed with a linear probe. The non-dominant hand of the patient will be fixed in the anatomical position on the arm chair. The wrist joint of patient will be extended to 30 degree with a wrist pad. The USG probe will be transversally placed 2 cm proximal to the styloid process and the short axes of the radial arter will be scanned. The diameter of the radial artery will be measured and recorded.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients will be operated under general anesthesia

  • patients were American Society of Anesthesiology (ASA) physical status I or II

Exclusion Criteria:
  • ASA III, IV, V

  • History of coroner artery disease

  • History of peripheral artery disease,

  • History of diabetes mellitus,

  • History of hypertension

  • Hemodynamic instability

  • Hypovolemia

  • History of Reynaud phenomenon

  • History of hand or arm trauma

  • previous catheterization

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul University Cerrahpasa Medical Faculty Istanbul Turkey

Sponsors and Collaborators

  • Istanbul University

Investigators

  • Principal Investigator: Güniz Meyancı Köksal, Prof., Istanbul University Cerrahpasa Medical Faculty

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Guniz M.Koksal, Prof. Dr., Istanbul University
ClinicalTrials.gov Identifier:
NCT03405428
Other Study ID Numbers:
  • 419999
First Posted:
Jan 23, 2018
Last Update Posted:
Mar 13, 2018
Last Verified:
Mar 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Guniz M.Koksal, Prof. Dr., Istanbul University

Study Results

No Results Posted as of Mar 13, 2018