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Vascular events In Surgery patIents cOhort evaluation-Cardiac Surgery

A large multicenter,international cohort study eveluating major vascular events in patients undergoing cardiac surgery - VISION Cardiac Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012906
Enrollment
15000
Registered
2018-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients who have undergone cardiac surgery

Interventions

Intervention1: NIL: NIL

Sponsors

Population Health Research Institution
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age > 18 years 2.Patients who have undergone cardiac surgery.This includes coronary artery bypass grafting and all open heart procedures such as valvular repairs/Replacement

Exclusion criteria

Exclusion criteria: 1.Previously enrolled in the VISION Cardiac Surgery 2.Patients who have undergone an isolated pericardial window,pericardiectomy,permanent pacemaker or defibrillator implantation

Design outcomes

Primary

MeasureTime frame
1.Primary Outcome: All-cause mortality at 30-days after surgery 2.Myocardial injuries that were not identified clinically during the first 5 days after surgery 3.Major vascular complications at 30-days and separately at 1-year after surgeryTimepoint: 2-5 DAYS,30 DAYS,1 YEAR FOLLOW UP—

Secondary

MeasureTime frame
Major vascular complications at 30-days after surgeryTimepoint: 30 days and 1 year—

Countries

Australia, Brazil, Canada, China, Hong Kong, India, Italy, Malaysia, Russian Federation, Spain, United Kingdom, United States of America

Contacts

Public ContactDr Alben Sigamani

Narayana Hrudayalaya Ltd

alben.sigamani.dr@narayanahealth.org8884431444

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026