RecruitingNot Applicable

Safety and Efficacy of CAG and PCI Via Distal Transradial Access in Patients With Small Vessels

China594 participantsStarted 2026-02-24

Plain-language summary

Randomized controlled trial of adaptive design for the safety and efficacy of coronary angiography and percutaneous coronary intervention via distal transradial access using a 6-French Glidesheath Slender in patients with small vessels.

Who can participate

Age range

18 Years – 85 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age between 18 and 85 years * Palpable pulses in both the distal radial artery and conventional radial artery * All patients signed informed consent forms prior to procedure Exclusion Criteria: * Ultrasound assessment of the distal radial artery diameter ≥2.0mm or \<1.0mm * Height ≥185.0cm * Patients with acute ST-segment elevation myocardial infarction, cardiogenic shock, or hemodynamic instability * Contraindications for puncture of the distal radial artery * Patients with Raynaud's syndrome * Patients with coagulation disorders or hematologic diseases * Patients currently enrolled in other clinical studies

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Distal radial artery occlusion(dRAO)

Timeframe: 24 hours postoperatively.

Trial details

NCT IDNCT07410364

SponsorCai gaojun, MD

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-02-01

Contact for this trial

gaojun GJ cai, PhD

+86 0519-85579192 caigaojun@wjrmyy.cn

View on ClinicalTrials.gov More Coronary Artery Disease trials

Who can participate

Age range

18 Years – 85 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.