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Clinical Trial 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).


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01997242
Study type Observational [Patient Registry]
Source Arcispedale Santa Maria Nuova-IRCCS
Contact Stefano Savonitto, MD
Phone +39-0341-489490
Email s.savonitto@ospedale.lecco.it
Status Recruiting
Phase N/A
Start date June 2013
Completion date September 2015

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