Italian Absorb Registry

NCT02298413 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1520

Last updated 2016-02-04

No results posted yet for this study

Summary

The investigators aim at evaluating the long-term (5-year) clinical outcome following Absorb BVS implantation in a real world, all-comers population of consecutive patients, as treated according to the indications, techniques and protocols used in the participating institutions.

Conditions

Interventions

DEVICE

PCI with Absorb scaffold

Implantation of biovascular scaffold during PCI

Sponsors & Collaborators

  • Fatebenefratelli and Ophthalmic Hospital

    collaborator OTHER
  • Bolognini Hospital

    collaborator UNKNOWN
  • Ospedale Regionale di Aosta

    collaborator UNKNOWN
  • Ospedali Riuniti di Ancona

    collaborator UNKNOWN
  • S. Giacomo Hospital

    collaborator OTHER
  • Azienda U.L.S.S n.9 Ospedale di Treviso Ca Foncello

    collaborator UNKNOWN
  • Ospedale San Bortolo di Vicenza

    collaborator OTHER
  • Azienda Ospedaliera Brotzu

    collaborator OTHER
  • San Giuseppe Moscati Hospital

    collaborator OTHER
  • Azienda Sanitaria Locale USL 13 Ospedale Mazzoni di Ascoli Piceno

    collaborator UNKNOWN
  • S. Andrea Hospital

    collaborator OTHER
  • Ospedale Monaldi di Napoli

    collaborator UNKNOWN
  • Azienda Ospedaliera di Padova

    collaborator OTHER
  • Ospedale della Misericordia di Grosseto

    collaborator UNKNOWN
  • Ospedale Santa Corona di Pietra Ligure

    collaborator UNKNOWN
  • Istituto Di Ricerche Farmacologiche Mario Negri

    collaborator OTHER
  • Ospedale Santa Croce-Carle Cuneo

    lead OTHER

Principal Investigators

  • Alfonso Ielasi, MD · AO Seriate

  • Bernardo Cortese, MD · AO Fatebenefratelli

  • Donatella Corrado, PhD · Istituto Di Ricerche Farmacologiche Mario Negri

Eligibility

Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2016-11-30
Completion
2021-05-31

Countries

  • Italy

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02298413 on ClinicalTrials.gov