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Recruiting Not applicable

Timing of Anticoagulant Administration During Radial Access Percutaneous Coronary Intervention: the HERA-PCI Study (Heparin Early for Radial Access Percutaneous Coronary Intervention)

NCT06890312 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-06-05
Last updated
2026-05-26

Condition(s) studied

Coronary AngiographyPercutaneous Coronary InterventionRadial Artery OcclusionBleedingAnticoagulation

Investigational drug(s) / intervention(s)

Administration of heparin after sheath insertionAdministration of heparin prior to sheath insertion

Administration of heparin after sheath insertion: Administration of heparin after sheath insertion

Administration of heparin prior to sheath insertion: Administration of heparin prior to sheath insertion

Study summary

While the reduced hemorrhagic risk of radial access for percutaneous coronary intervention compared to femoral access is well-established, its main complication remains radial artery occlusion, which can occur in up to 30% of patients. Anticoagulation is the primary preventive measure recommended in clinical practice to reduce the risk of this complication, typically involving heparin injection during the procedure in most centers. However, data on the effect of the timing of heparin injection are limited. The investigators hypothesize that injection of heparin before sheath insertion may reduce the rate of radial artery occlusion compared with injection after sheath insertion.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients having 18 years old or older, regardless of gender, undergoing percutaneous radial coronary intervention * Subject affiliated to a social protection health insurance * Subject able to understand the objectives and risks of the research and to provide dated and signed consent * Subject who has been informed of the results of the preliminary medical examination Exclusion Criteria: * Contraindication to the use of heparin (history of heparin-induced thrombocytopenia) * Very high bleeding risk defined by recent bleeding (\<6 months) of type 3 of the BARC classification * Subject in an exclusion period (determined by a previous or ongoing study) * Inability to give the subject enlightened information (subject in an emergency situation, difficulties in understanding the subject, etc.) * Subject under safeguard of justice * Subject under guardianship or curatorship * Pregnancy * Breastfeeding * Patient on anticoagulant treatment: anti-vitamin K, direct oral anticoagulants (DOACs).

Primary outcome measure(s)

  • Rate of radial artery occlusion — Day 1
    The primary endpoint is the rate of radial artery occlusion, as determined by Doppler ultrasound at day 1.

Trial sites (1)

FacilityCityRegionStatus
Hôpitaux Universitaires de Strasbourg Strasbourg Bas-Rhin Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06890312 on ClinicalTrials.gov ↗ ← All trials in France