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New training method could help doctors master artery access

NCT ID NCT07248683

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Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
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When the status isn't known

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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a new teaching method helps medical students learn how to insert a small tube into the wrist artery. The method uses ultrasound to guide the needle and spaced repetition practice. Thirty resident doctors will be split into two groups to compare the new approach with standard training. The goal is to see if the new method leads to more successful first attempts and fewer complications.

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Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Nov 2025

An estimate. Start dates often move.

Expected to finish

Feb 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion and Exclusion Criteria for Study Participants (Resident Trainees) I. Inclusion Criteria Identity and Qualifications: Resident physicians undergoing standardized training in this department. Training Stage: Resident physicians who have not yet independently performed ultrasound-guided radial artery puncture and catheterization procedures. Willingness to Learn: Voluntary participation in this "Ultrasound-Guided Radial Artery Catheterization" training program with full understanding of the research content. Informed Consent: Have signed a written informed consent form agreeing to participate in this study and comply with protocol requirements. Basic Requirements: Possess good hand-eye coordination and learning ability, capable of cooperating to complete the entire training course and data collection. II. Exclusion Criteria Prior Experience: Residents who have previously independently completed more than 5 cases or have systematically studied ultrasound-guided radial artery puncture and catheterization techniques. Skill Level: Residents who achieved a high pre-test performance score or demonstrated consistent success in performing ultrasound-guided radial artery catheterization prior to the study. Cognitive or Motor Impairment: Residents with severe cognitive dysfunction, motor impairment, or a history of psychiatric disorders that may compromise training efficacy assessment. Time Commitment and Compliance: Individuals unable to guarantee completion of the prescribed training program, practical exercises, and follow-up evaluations. Other Conditions: Participants deemed unsuitable for this study by the investigator due to other reasons (e.g., rotation schedule conflicts, inability to coordinate personal time, etc.). Inclusion and Exclusion Criteria for Study Subjects (Patients Undergoing Radial Artery Catheterization) I. Inclusion Criteria Age: Generally ≥18 years old. Clinical Indications: Patients requiring invasive arterial pressure monitoring via radial artery puncture and catheterization due to surgical procedures, critical condition monitoring, or blood gas analysis. Vascular Criteria: Palpable radial artery pulse on the puncture side, negative modified Allen test (or adequate ulnar artery compensation as determined by current guidelines). Informed Consent: Patient or authorized family member fully understands the study purpose and procedures, and has signed a written informed consent form. Cooperation Capacity: Able to cooperate throughout the radial artery puncture and catheterization procedure. II. Exclusion Criteria Contraindications for Puncture: History of thrombosis, aneurysm, or arteriovenous fistula at the puncture site; skin infection, laceration, burn, or severe scar tissue at the puncture site. Circulatory Impairment: Severe shock, hypovolemic state, or anticipated difficulty with radial artery puncture. Coagulation Abnormalities: Significant bleeding tendency, marked thrombocytopenia, or ongoing anticoagulant/antiplatelet therapy without discontinuation. Abnormal vascular anatomy: Preliminary ultrasound assessment indicates severe tortuosity, malformation, excessively narrow diameter, or other significant anatomical variations in the radial artery that may compromise puncture success or safety. Special circumstances: Requirement for simultaneous bilateral radial artery catheterization; or other situations deemed unsuitable for this teaching procedure by the investigator.

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As listed by the trial registrant

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