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NCT07256249Recruiting

Real-life Registry in Patients With Coronary Artery Disease Treated With the SELUTION Sirolimus-eluting Balloon. Selution Iberia Registry

Source: ClinicalTrials.gov · Last updated 29 Oct 2026

Brief summary (registry, in English)

Selution Iberia registry is a post-market clinical follow-up, prospective, multicenter, international, longitudinal, observational study without a control group of consecutive unselected "real-world" patients with coronary artery disease in whom it was decided to use the SELUTION SLRTM device in the treatment of primary native lesions and ISR (in-stent restenosis) in all settings, in order to evaluate its effectiveness and safety. The primary objective is to evaluate the effectiveness and safety of the Sirolimus-eluting balloon SELUTION SLRTM based strategy in the treatment of native coronary artery stenosis and in-stent restenosis. The primary endpoint will be the incidence of major adverse cardiovascular events at 12 months, including death, non-fatal myocardial infarction or target lesion revascularization for ischemia, in an unselected "real-world" patient setting. Both Device Oriented Composite Endpoint (Cardiovascular death, device failure-related myocardial infarction or device failure-related ischaemia) and Patient Oriented Composite Endpoint (all cause death, any stroke, any myocardial infarction or any revascularization) will be detailed.

Status (registry)
Recruiting
Study type
Observational
Enrollment
960 (estimated)
First submitted
20 Nov 2025
Start date
11 Dec 2025
Primary completion date
31 Dec 2026
Lead sponsor
Fundación EPIC
NCT number
NCT07256249

What you commit to

  • Study type: Observational
  • Planned participants: 960
  • From 11 Dec 2025 to the primary completion date, 31 Dec 2026
  • 16 sites in 2 countries
  • 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

  • Express refusal of the patient to participate in the study
  • Life expectancy of the patient of less than 12 months

Who the study is looking for

  • Patients with age ≥18 years and;
  • Patients with coronary artery disease in whom, at the operator's discretion, treatment of a lesion in a native vessel, coronary graft or coronary restenosis is decided using the Selution SLRTM device;
  • Patient who has been informed of the characteristics of the study and has provided written informed consent.

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

Full criteria on ClinicalTrials.gov

Sites (16)

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

SiteCityCountrySite status
Hospital Universitari Germans Trias i Pujol
Coordinator of this site? Confirm its status
BadalonaSpainRecruiting
Hospital de la Santa Creu i Sant Pau
Coordinator of this site? Confirm its status
BarcelonaSpainRecruiting
Hospital del Mar
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BarcelonaSpainRecruiting
Hospital Universitario De Leon
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LeónSpainRecruiting
Hospital Universitario de Canarias
Coordinator of this site? Confirm its status
San Cristóbal de La LagunaSpainRecruiting
Hospital Universitario Marqués de Valdecilla
Coordinator of this site? Confirm its status
SantanderSpainRecruiting
Hospital Clínico Universitario de Santiago
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Santiago de CompostelaSpainRecruiting
Hospital Universitario Virgen del Rocio
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SevilleSpainRecruiting
Hospital Universitari MutuaTerrassa
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TerrassaSpainRecruiting
Hospital Universitario de Torrevieja
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TorreviejaSpainRecruiting
Hospital Universitario de Pontevedra
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Vilagarcía de ArousaSpainRecruiting
Hospital Prof. Doutor Fernando da Fonseca
Coordinator of this site? Confirm its status
AmadoraPortugalRecruiting
Hospital de Santa Cruz
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CarnaxidePortugalRecruiting
Hospital Universitário de Coimbra
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CoimbraPortugalRecruiting
Hospital de Faro
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FaroPortugalRecruiting
ULS TAMEGA e SOUSA
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PenafielPortugalRecruiting

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