PREVAIL Paclitaxel-coated Balloon in Small Coronary Disease and High-bleeding Risk Patients

Last updated: February 13, 2025
Sponsor: Fundación EPIC
Overall Status: Active - Recruiting

Phase

N/A

Condition

Myocardial Ischemia

Thrombosis

Atherosclerosis

Treatment

Percutaneous Coronary Intervention with DCB and DAPT

Clinical Study ID

NCT06321757
EPIC30-PARIS
  • Ages > 18
  • All Genders

Study Summary

Post-market, prospective, observational, multicenter, non-intervention study, to demonstrate the effectiveness of drug-coated ballon (DCB)therapy in real-world patients with small native vessel coronary artery disease, and to demonstrate the safety of short dual antiplatelet therapy (7 days) in high-bleeding risk patients with native small vessel coronary artery disease treated with DCB therapy. A percutaneous coronary intervention (PCI) with DCB will be performed in patients with native vessel coronary artery disease based on the criterion of the treating physician.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patients with:

  • PCI with DCB on native arteries with diameters < 3 mm.

  • Indication for PCI in acute coronary syndrome or chronic coronary syndrome or silentangina with an indication for PCI.

syndrome or silent angina with an indication for PCI.

  • If previous lesion preparation was required after which angiographic residual lesionshould not exist with diameter stenosis > 30% or flow-limiting coronary dissections.

  • All antithrombotic therapies administered prior to the procedure are accepted.Still, they can be changed after the procedure.

  • Capacity to understand and sign the written informed consent.

  • If the patient has a high-bleeding risk defined by 1) PRECISE-DAPT SCORE ≥ 25 or 2)an indication for concomitant oral anticoagulation he can be included in the high-bleeding risk substudy as long as he does not meet the specific exclusion criteria.

Exclusion

Exclusion Criteria:

Patients with:

  • Concomitant lesions on vessels > 3 mm in diameter in the same coronary territory.

  • PCI on in-stent restenoses.

  • PCI on culprit lesions of acute coronary syndrome with ST segment elevation.

  • Patients with an indication for PCI on additional non-culprit lesions of acutecoronary syndrome with ST segment elevation may be included in the study, if onlynon-culprit lesions are considered for the study.

  • Life expectancy <12 months

  • Pregnancy.

  • Participation in clinicaltrials.

  • Inability to give the written informed consent.

  • Specific exclusion criteria for the high-bleeding risk patient subgroup:

  • Past medical history of stent thrombosis.

  • Indication for dual antiplatelet therapy for a different reason.

Study Design

Total Participants: 501
Treatment Group(s): 1
Primary Treatment: Percutaneous Coronary Intervention with DCB and DAPT
Phase:
Study Start date:
February 26, 2024
Estimated Completion Date:
December 30, 2026

Study Description

Post-market, prospective, multicenter, non-intervention study, to demonstrate the effectiveness of drug-coated ballon therapy in real-world patients with small native vessel coronary artery disease, and to demonstrate the safety of short dual antiplatelet therapy (7 days) in high-bleeding risk patients with native small vessel coronary artery disease treated with DCB therapy. A PCI with DCB will be performed in patients with native vessel coronary artery disease based on the criterion of the treating physician. The angiographic study will be analyzed in a core lab (icicorelab) blinded to the procedural outcomes and the patients' follow-up.

As per clinical practice, 1-year clinical follow-up of all the patients will be conducted with a first assessment at 30 days, a second assessment at 6 months, and one final assessment at 12 months.

Should the patient have an elevated bleeding risk -defined as concomitant therapy with oral anticoagulation or a PRECISE-DAPT score ≥ 25- patients will be included in a high-bleeding risk substudy. The antiplatelet therapy regime will be administered according to the local investigator and the treating medical team.

Connect with a study center

  • Hospital General Universitario de Albacete

    Albacete, 02008
    Spain

    Active - Recruiting

  • Hospital Universitario de Cruces

    Barakaldo, 49803
    Spain

    Active - Recruiting

  • Hospital General Universitario de Ciudad Real

    Ciudad Real, 13005
    Spain

    Active - Recruiting

  • Hospital Universitario Clinico San Cecilio

    Granada, 18016
    Spain

    Active - Recruiting

  • Hospital Universitari de Bellvitge

    Hospitalet de Llobregat, 08907
    Spain

    Active - Recruiting

  • Hospital Universitario Juan Ramon Jimenez

    Huelva, 21005
    Spain

    Active - Recruiting

  • Hospital Universitario de Gran Canaria Doctor Negrín

    Las Palmas De Gran Canaria, 35010
    Spain

    Active - Recruiting

  • Hospital Universitario de Leon

    León, 24071
    Spain

    Active - Recruiting

  • Hospital Universitario de La Princesa

    Madrid, 28006
    Spain

    Active - Recruiting

  • Hospital Universitario Virgen del Rocío

    Sevilla, 41013
    Spain

    Active - Recruiting

  • Hospital Universitario Y Politecnico La Fe

    Valencia, 46026
    Spain

    Active - Recruiting

  • Hospital Clinico Universitario de Valladolid

    Valladolid, 47003
    Spain

    Active - Recruiting

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