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NCT06787287Completed

A Study on the Application of Simple and Improved Radial Artery Compression Method After Transradial Coronary Intervention

A Study on the Application of Simple and Improved Radial Artery Compression Method After Transradial Coronary Intervention A Randomized, Controlled Clinical Trial

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

The objective of this study was to evaluate the specific effect of a simple modified method of thick gauze (9cm\*16cm\*8mm) combined with a hemostatic device in the prevention of early radial artery occlusion and other related vascular complications after transradial coronary intervention.

Status (registry)
Completed
Study type
Interventional
Enrollment
1624 (actual)
First submitted
10 Jan 2025
Start date
31 Jul 2023
Primary completion date
30 Apr 2025
Lead sponsor
Guozhe Sun
NCT number
NCT06787287

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1624
  • From 31 Jul 2023 to the primary completion date, 30 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with blood or liver diseases;
  • Patients with vascular diseases or malformations in the forearm;
  • Patients with a history of RAO at baseline of the radial artery on the approach;
  • Approach side arteriovenous fistula dialysis patients;
  • Patients with subclavian artery occlusive disease (definite medical history or the difference in systolic blood pressure between the two upper limbs is more than 20mmHg);
  • Active bleeding at the puncture site before extraction;

Other

  • Intraoperative Allen test was positive for all patients;
  • The intraoperative Barbeau tests were all D grade radial artery patients;
  • Patients who have completed coronary intervention (full heparin);
  • Systolic blood pressure greater than 180 mm Hg or diastolic blood pressure greater than 110 mm Hg at closure;
  • Pregnant women or patients who are trying to conceive and have family plans;
  • Patients whom the investigator deems inappropriate to participate in the clinical trial;

Who the study is looking for

  • Over 18 years old, regardless of gender;
  • Patients undergoing coronary intervention;
  • Patients with a transradial approach;
  • Voluntarily participate and sign informed consent;

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
First Hospital of China Medical University
Coordinator of this site? Confirm its status
ShenyangChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.