Ultrathin Strut Sirolimus-eluting Stent With Bioabsorbable Polymer in Patients Receiving Chronic Oral Anticoagulation

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

Patients receiving chronic oral anticoagulation with indication for percutaneous coronary revascularization with stent implantation, and needing for antiplatelet therapy, are at high risk of bleeding. The new generation of ultrathin strut sirolimus-eluting stent with bioabsorbable polymer allow for shorter antiplatelets regimens and could be a good option for this high-bleeding risk patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Patients must meet all inclusion criteria:

• Patients with Signed informed consent and

• Patients with \>=18 years old and

• Patients with chronically receiving oral anticoagulation treatment with any type of anticoagulant for any reason and

• Patients with de novo Coronary artery disease requiring both elective or urgent percutaneous revascularization due to stable coronary artery disease or acute coronary syndrome with or without ST-segment elevation, and in which an ultrathin strut Sirolimus-eluting stent with bioabsorbable polymer has been used

Locations
Other Locations
Spain
Hospital General Universitario de Albacete
RECRUITING
Albacete
Hospital Universitario San Juan de Alicante
RECRUITING
Alicante
Hospital General Universitario de Merida
RECRUITING
Badajoz
Hospital General Universitari de Castelló
RECRUITING
Castelló
H.G.U. de Ciudad Real.
RECRUITING
Ciudad Real
Hospital General Universitari d'Elx
RECRUITING
Elche
Hospital Universitario Puerta de Hierro
RECRUITING
Majadahonda
Hospital Clinico Universitario Lozano Blesa
RECRUITING
Zaragoza
Contact Information
Primary
Juan Gabriel Córdoba Soriano, MD, PhD
jgcordoba@foroepic.org
0034 967597532
Backup
FUNDACION EPIC
iepic@fundacionepic.org
0034987876135
Time Frame
Start Date: 2025-05-06
Estimated Completion Date: 2029-03-31
Participants
Target number of participants: 500
Treatments
Supraflex Cruz Sirolimus-eluting Stent
Sponsors
Leads: Fundación EPIC

This content was sourced from clinicaltrials.gov