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The Surgery After Stenting (SAS) Registry

NCT01997242 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2025-06-26

No results posted yet for this study

Summary

The SAS registry will include any patient with previous coronary stenting undergoing any type of surgery or operative endoscopic/endovascular procedure at the participating Centers. The relevant clinical, procedural and outcome data (within index surgical admission and at 30 days) will be entered in a specifically designed electronic case record form (eCRF).

Conditions

  • PERCUTANEOUS CORONARY INTERVENTION
  • STENTS
  • SURGERY

Sponsors & Collaborators

  • Italian Society of Invasive Cardiology

    collaborator OTHER

  • Associazione Nazionale Medici Cardiologi Ospedalieri

    collaborator OTHER

  • Azienda USL Reggio Emilia - IRCCS

    lead OTHER_GOV

Principal Investigators

  • Stefano Savonitto, MD · Division of Cardiology, Manzoni Hospital, Lecco

  • Roberta Rossini, MD · Cardiovascular Dpt, Ospedali Riuniti di Bergamo

  • Giovanni Tortorella, MD · Arcispedale Santa Maria Nuova - IRCCS, Reggio Emilia

  • Marco Ferri, MD · Arcispedale Santa Maria Nuova - IRCCS, Reggio Emilia

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-10
Primary Completion
2014-12-31
Completion
2014-12-31

Countries

  • Italy

Study Locations

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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 NCT01997242 on ClinicalTrials.gov