Ultrasonographic Evaluation of Arteries of the Hand in Pediatric Patients

April 24, 2025 updated by: Ozlem Can, Ankara University

Comparison of Ultrasonographic Measurements of Radial and Ulnar Arteries in Pediatric Patients Undergoing Elective Surgery

Ultrasound measurements of the ulnar artery and radial artery at different angles are obtained and compared to determine the optimal diameters for possible arterial cannulation in pediatric patients.

Study Overview

Status

Recruiting

Detailed Description

Radial artery cannulation is the most commonly used technique for invasive arterial catheterization in pediatric patients. Ultrasound guidance has significantly reduced cannulation success rates and complication risks. The ulnar artery presents an anatomical alternative to the radial artery and has emerged as a potential cannulation site. This study aims to comprehensively evaluate the suitability of the radial or ulnar artery for cannulation in pediatric patients.

Finding of this study objectives are

To obtain a large sample of pediatric patients from different age groups To measure arterial diameters using ultrasound at different angles and with ultrasound and to assess the optimal artery and the angle.

Study Type

Observational

Enrollment (Estimated)

184

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Ankara, Turkey, 06100
        • Recruiting
        • Ankara University School of Medicine
        • Contact:
        • Principal Investigator:
          • Ozlem S Can, MD
        • Sub-Investigator:
          • Zeynep S Altinbas, MD

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

  • Child

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Between 0 and 10 years of ages pediatric patients scheduled for elective surgery under general anesthesia

Description

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) physical status 1 or 2
  • Patients scheduled for elective surgical procedures
  • Informed consent must be obtained from both the patient and, if applicable, their parent or guardian.

Exclusion Criteria:

  • Patients over 10 years of age
  • Patients with congenital anomalies or syndromic conditions
  • Abnormal Allen Test
  • Skin Erosion or infection at the cannulation site
  • Hematoma at the cannulation 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Determining the Diameter and Depth at different angles
Time Frame: only once
The study aims to measure the radial and ulnar arteries using ultrasound at different angles to determine the widest diameter and the optimal angle to achieve this diameter.
only once
Comparing Ulnar and Radial Artery Diameters Across Age Groups
Time Frame: only once
Investigating whether there is a difference (ulnar>radial, ulnar=radial, or radial>ulnar) in the diameter of the ulnar artery compared to the radial artery among the age groups included in the study
only once

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

May 15, 2023

Primary Completion (Estimated)

May 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

April 23, 2024

First Submitted That Met QC Criteria

April 23, 2024

First Posted (Actual)

April 26, 2024

Study Record Updates

Last Update Posted (Actual)

April 27, 2025

Last Update Submitted That Met QC Criteria

April 24, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • USG for ped art can

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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