The Surgery After Stenting (SAS) Registry

A Multicenter Registry of Consecutive Patients Undergoing Cardiac and Noncardiac Surgery or Operative Endoscopic/Endovascular Procedures After Implantation of a Coronary Stent

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01997242

Acronym

SAS registry

Enrollment

Registered

2013-11-28

Start date

2013-06-10

Completion date

2014-12-31

Last updated

2025-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PERCUTANEOUS CORONARY INTERVENTION, STENTS, SURGERY

Keywords

CORONARY STENT, CARDIAC SURGERY, NON CARDIAC SURGEY

Brief 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).

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Eligible will be male and female patients \> 18 years of age. * Eligible will be patients with previous coronary stenting undergoing any kind of surgical or operative endoscopic procedure at the participating Centers, irrespective of the distance in time between stenting and surgery. * Both candidates to elective/urgent operations and those undergoing emergency operations will be included in the SAS registry, and will be considered as two separate cohorts.

Exclusion criteria

\- Unwillingess/inability to sign the Informed Consent Form (ICF). There are no other selection criteria.

Design outcomes

Primary

Measure	Time frame
The composite of death, myocardial infarction, probable/definite stent thrombosis according the Academic Research Consortium definition and bleeding events of Bleeding Academic Research Consortium (BARC)grade >3 during index surgical admission.	within the first 30 days after surgery

Secondary

Measure	Time frame
The incidence of bleeding events of Bleeding Academic Research Consortium (BARC) grade >3 within 30 days of index admission/procedure	within the first 30 days after surgery

Countries

Italy

Outcome results