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Modified Dynamic Needle Tip Positioning vs Conventional Long-axis In-plane in Radial Artery Cannulation

Modified Dynamic Needle Tip Positioning Versus Long-Axis In-Plane Ultrasound Guided Radial Artery Cannulation in Patients With Coronary Artery Disease: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05687370
Enrollment
124
Registered
2023-01-18
Start date
2023-01-15
Completion date
2023-03-26
Last updated
2023-03-30

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

Conditions

Arterial Catheterization, Coronary Artery Disease, Ultrasound

Brief summary

Conventionally, long-axis in-plane (LA-IP), short-axis out-of-plane (SA-OOP) and dynamic needle tip positioning based on SA-OOP views are commonly used method to image the target vessel during cannulation under US guidance. A modified SA-OOP that add developing line on the ultrasonic probe improve the success rate of cannula insertion into the radial artery on the first attempt.

Interventions

PROCEDUREModified dynamic needle tip positioning under ultrasound-guidance

The tip of needle is positioned under ultrasound-guidance using modified dynamic short-axis view.

The tip of needle is positioned under ultrasound-guidance using conventional long-axis in-plane view.

Sponsors

Qianfoshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. The diagnostic criteria of coronary atherosclerotic heart disease according to the tenth version of international Classification of diseases(ICD-10); 2. Requires invasive arterial blood pressure monitoring; 3. New York Heart Association(NYHA) classification I, II or III; 4. The American Society of Anesthesiologists (ASA) classification I, II or III; 5. Patients older than 18 years and younger than 85 years (Adult); 6. Patients signed the informed consent before the study.

Exclusion criteria

1. Patients with hemodynamically unstable (systolic blood pressure 60 or less); 2. Patients with abnormal results of the modified Allen test; 3. Patients with ulnar artery occlusion; 4. Patients with coagulation disorders; 5. Patients with skin abnormalities such as inflammation or hematoma at the cannulation site; 6. Patients with raynaud disease and prevalent atherosclerosis; 7. Patients with history of hand or wrist trauma or surgery; 8. Patients who have undergone radial artery interventional therapy or radial artery cannulation within 3 months on the puncture side; 9. Patients with BMI more than 40 kg/m2; 10. Patients who have participated in other relevant clinical studies within 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Success rate of the radial artery cannulation at first attemptintraoperativeSuccessful confirmation of the arterial waveform through a pressure monitor at first attempt of the radial artery cannulation

Secondary

MeasureTime frameDescription
Time of arterial catheterizationInterval between contact of the ultrasound transducer with the skin and confirmation of an arterial waveform on the monitor, an expected average observation time of 300 seconds
Time to first puncture of the arteryInterval between skin penetration of the needle and flashback of blood, an expected average of 200 seconds
Time ultrasound imagingInterval between contact of the ultrasound transducer with the skin and penetration of the needle through the skin, , an expected average of 100 seconds
Number of puncture attemptsUp to 5 times, an expected average observation time of 70 seconds
Vascular complications in the surgerypostoperative, within 24 hoursincluding thrombosis, hematoma, and vasospasm

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026