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NCT03263260Completed

Post-marketing Registry of Inspiron Sirolimus Eluting Coronary Stent

Prospective, Multicentric, Post-marketing Registry of Inspiron Sirolimus Eluting Coronary Stent for Treatment of Patients With Native Coronary Artery Lesions (Inspiron Real Life II)

Source: ClinicalTrials.gov · Last updated 4 Sept 2024

Brief summary (registry, in English)

Post-marketing, prospective, multicentric, non-randomized registry to evaluate the safety and efficacy of Inspiron Sirolimus Eluting Coronary Stent at the treatment of "real-world" patients.

Status (registry)
Completed
Study type
Observational
Enrollment
2504 (actual)
First submitted
24 Aug 2017
Start date
2 Jun 2017
Primary completion date
15 Dec 2022
Lead sponsor
Scitech Produtos Medicos SA
NCT number
NCT03263260

What you commit to

  • Study type: Observational
  • Participants enrolled: 2504
  • From 2 Jun 2017 to the primary completion date, 15 Dec 2022
  • 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

  • Safein Vein or Left Internal Mammary artery Grafts

Who the study is looking for

  • alll patients that have been treated with the Inspiron Sirolimus Eluting Stent older and 18 years

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
União Brasileira de Educação e Assistência - Hospital São Lucas da PUC - RS
Coordinator of this site? Confirm its status
Porto AlegreBrazilUnknown status

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