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Comparison of the application of bracket assisted laser-guide with long-axis in-plane ultrasound guidance in radial artery cannulation:a randomized controlled trial

Comparison of the application of bracket assisted laser-guide with long-axis in-plane ultrasound guidance in radial artery cannulation:a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086128
Enrollment
Unknown
Registered
2024-06-25
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

radial artery cannulation

Interventions

bracket assisted laser-guide group:radial artery cannulation using the bracket assisted laser-guide method
long-axis in-plane group:using long-axis in-plane ultrasound guidance for radial artery cannulation

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. The patient fully understands and voluntarily participates in this study, signing an informed consent form 2. Select surgical patients who require continuous monitoring of blood pressure through radial artery puncture and catheterization 3. ASA classification is level I-IV 4. Patients aged 18 or above, no gender limited

Exclusion criteria

Exclusion criteria: 1. Patients who have undergone radial artery cannulation within one month 2. Patients with radial and ulnar arteries a anomalies, peripheral vascular diseases at the site of radial artery puncture, congenital heart disease, hemorrhagic or cardiogenic shock 3. Wounds, infections, and hematomas near the puncture site of the radial artery 4. Insufficient collateral circulation or negative Allen test 5. The situation which patients refuse to sign informed consent to participate in this study 6. Other situations which its unsuitable to participate in this study

Design outcomes

Primary

MeasureTime frame
first attempt success rate;

Secondary

MeasureTime frame
procedure time to success within first attempt;Success rate within two attempts in less than 10 min;Procedure time to success within the second attempt;Number of unintentional penetrating the posterior wall;Average number of adjustments;Overall success rate;Use of another puncture site;Use of the transfixion technique;Overall procedure time;Overall number of attempts;

Countries

China

Contacts

Public ContactLi Zhiwen

The First Hospital of Jilin University

lizhiwen@jlu.edu.cn+86 188 4317 7788

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026