ClinicalTrials.gg
RecruitingNCT07801807Updated Sep 3, 2026

Short-Axis Versus Long-Axis Ultrasound-Guided Radial Artery Cannulation

An interventional study of Short-Axis/Out-of-Plane Radial Artery Cannulation and Long-Axis/In-Plane Radial Artery Cannulation in Radial Artery Cannulation, sponsored by Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital. Recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-03.

Sponsored by Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
144
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This randomized controlled study aims to compare short-axis/out-of-plane and long-axis/in-plane ultrasound-guided techniques for radial artery cannulation in adult patients undergoing elective surgery. The study will also investigate whether the depth of the radial artery from the skin is associated with cannulation success and may help guide the selection of the ultrasound-guided cannulation technique.

Participants will be randomly assigned to either the short-axis/out-of-plane group or the long-axis/in-plane group. Radial artery depth will be measured using ultrasound before cannulation. The two techniques will be compared in terms of cannulation success, including first-attempt success, number of punctures and needle redirections, time to successful cannulation, failed cannulation, and procedure-related complications.

02

Conditions studied

  • Radial Artery Cannulation

Keywords

  • Radial artery cannulation
  • Ultrasound guidance
  • Short-axis approach
  • Out-of-plane technique
  • Long-axis approach
  • In-plane technique
  • Radial artery depth
  • Arterial catheterization
03

In context

Lead sponsor

Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital is the lead sponsor of 59 studies on the registry; 25 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

nclusion Criteria:

Age 18 years or older Patients with an indication for radial artery cannulation for invasive arterial monitoring Undergoing a surgical or interventional procedure Radial artery suitable for visualization by ultrasound Provision of written

Exclusion Criteria:

Age younger than 18 years Infection, burn, scar, or skin lesion at the planned cannulation site Previous vascular surgery involving the study extremity Advanced peripheral arterial disease or radial artery occlusion Inadequate collateral circulation as assessed by the Allen test or ultrasound Severe coagulopathy Presence of an arteriovenous fistula in the study extremity Severe hemodynamic instability Multiple previous failed radial artery cannulation attempts in the same extremity Pregnancy Allergy to ultrasound gel Refusal to participate in the study

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
144 participants (estimated)

Study arms

  • Experimental
    Short-Axis/Out-of-Plane Approach

    Participants assigned to this group will undergo ultrasound-guided radial artery cannulation using the short-axis/out-of-plane approach.

    Procedure: Short-Axis/Out-of-Plane Radial Artery Cannulation

  • Active comparator
    Long-Axis/In-Plane Approach

    Participants assigned to this group will undergo ultrasound-guided radial artery cannulation using the long-axis/in-plane approach.

    Procedure: Long-Axis/In-Plane Radial Artery Cannulation

Interventions

  • ProcedureShort-Axis/Out-of-Plane Radial Artery Cannulation

    Ultrasound-guided radial artery cannulation will be performed using the short-axis/out-of-plane approach. The radial artery will be visualized in the short-axis view, and the needle will be advanced using an out-of-plane technique until successful arterial cannulation.

  • ProcedureLong-Axis/In-Plane Radial Artery Cannulation

    Ultrasound-guided radial artery cannulation will be performed using the long-axis/in-plane approach. The radial artery will be visualized in the long-axis view, and the needle will be advanced using an in-plane technique until successful arterial cannulation.

06

What researchers measure

Primary outcomes

  1. Success Rate of Short-Axis/Out-of-Plane Versus Long-Axis/In-Plane Radial Artery Cannulation

    The success rates of ultrasound-guided radial artery cannulation using the short-axis/out-of-plane and long-axis/in-plane approaches will be compared. Successful cannulation is defined according to the study protocol as successful radial artery catheter placement within the predefined procedural criteria.

    Time frame: During the radial artery cannulation procedure

Secondary outcomes

  1. First-Attempt Cannulation Success

    Time frame: During the radial artery cannulation procedure

Other outcomes

  1. Number of Puncture Attempts

    Time frame: Time to Successful Radial Artery Cannulation

  2. Procedure-Related Complications

    Time frame: During the radial artery cannulation procedure

  3. Number of Needle Redirections

    Time frame: During the radial artery cannulation procedure

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07801807
Lead sponsor
Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital
Responsible party
Fikret Salık (Dicle University, Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital) — Principal investigator
First posted
Sep 3, 2026
Start date
Aug 25, 2026 (estimated)
Primary completion
Dec 15, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Sep 3, 2026

Study contacts

Fikret Salik, MD
Contact
fikretsalik@gmail.com
+90 507 621 4125
Fikret Salik, MD
principal investigator · Dicle University Faculty of Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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