Skip to content

Distal or Conventional Transradial Access Site for Primary Percutaneous Coronary Intervention-a Randomized Clinical Trial

Distal or Conventional Transradial Access Site for Primary Percutaneous Coronary Intervention-a Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061841
Enrollment
Unknown
Registered
2022-07-03
Start date
2022-01-05
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

ST segment elevation myocardial infarction

Interventions

experimental group:distal radial artery
control group:conventional radial artery

Sponsors

Beijing Luhe Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients older than 18 years; 2. Onset time within 24 hours ang plan for primary percutaneous coronary intervention; 3. The presence of a perceptible pulse from the radial artery in its proximal and distal segments; 4. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Unstable clinical status; 2. Severe renal insufficiency without Renal replacement therapy; 3. The absence of a perceptible pulse from the radial artery in its proximal and distal segments; 4. Allergic to iodinated contrast media; 5. Contraindications to antiplatelets and anticoagulation; 6. Pregnant.

Design outcomes

Primary

MeasureTime frame
radial aretry occlusion;

Secondary

MeasureTime frame
the rate of successful sheath insertion;time of sheath insertion;first medical contact to balloon time;rates of vascular access complications;major adverse cardiac events;the rate of procedure success;radial artery occlusion;

Countries

China

Contacts

Public ContactJincheng Guo

Beijing Luhe Hospital

Guojcmd@126.com+86 13521968844

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026