Skip to main content
TTrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor.
RECRUITINGOBSERVATIONAL

Vascular Events In Patients Undergoing Same-day Noncardiac Surgery (VALIANCE) Study

Vascular Events In Patients Undergoing Same-day Noncardiac Surgery (VALIANCE) Study - A Prospective Observational Cohort Study Evaluating Major Cardiovascular and Adverse Events in Patients Undergoing Elective Same-day Noncardiac Surgery

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The proportion of noncardiac surgeries performed as same-day surgery is increasing worldwide, with more complex surgeries being performed on higher risk patients in the outpatient setting. Little is known on the risk factors, incidence and prognosis of patients undergoing same-day noncardiac surgery. The main objective of this study is to inform on the incidence and risk factors of cardiovascular and other adverse events after same-day surgery and to develop risk prediction tools to better inform on the risk and selection of patients undergoing same-day surgery.

Who May Be Eligible (Plain English)

Who May Qualify: - 45-64 years of age with at least one risk factor, or ≥65 years of age; - undergoing elective noncardiac same-day surgery; - planned duration in the operating room 60 minutes or more; - provided written consent. Who Should NOT Join This Trial: - intervention does not require the presence of an anesthesiologist; - procedure is performed by a nonsurgical specialty (e.g., gastroenterology, pneumology, radio-oncology or radiology); - intervention is an ophthalmologic procedure; - previously enrolled in the VALIANCE study. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 45-64 years of age with at least one risk factor, or ≥65 years of age; * undergoing elective noncardiac same-day surgery; * planned duration in the operating room 60 minutes or more; * provided written consent. Exclusion Criteria: * intervention does not require the presence of an anesthesiologist; * procedure is performed by a nonsurgical specialty (e.g., gastroenterology, pneumology, radio-oncology or radiology); * intervention is an ophthalmologic procedure; * previously enrolled in the VALIANCE study.

Locations (16)

Wake Forest Baptist Medical Centre
Winston-Salem, North Carolina, United States
Cleveland Clinic Foundation Fairview Campus
Cleveland, Ohio, United States
Cleveland Clinic Foundation Main Campus
Cleveland, Ohio, United States
MD Anderson Cancer Center
Houston, Texas, United States
Memorial Hermann Texas Medical Center UT Health
Houston, Texas, United States
St-Joseph's Healthcare Hamilton
Hamilton, Ontario, Canada
Hamilton General Hospital
Hamilton, Ontario, Canada
Juravinski Hospital and Cancer Centre
Hamilton, Ontario, Canada
McMaster University Medical Centre
Hamilton, Ontario, Canada
Mount Sinai Hospital
Toronto, Ontario, Canada
Toronto Western Hospital
Toronto, Ontario, Canada
St-Micheal's Hospital
Toronto, Ontario, Canada
Centre Hospitalier de l'Université de Montréal (CHUM)
Montreal, Quebec, Canada
Centre Hospitalier Universitaire de Sherbrooke
Sherbrooke, Quebec, Canada
Maasstad Ziekenhuis Rotterdam
Rotterdam, Netherlands
Hospital Clinic Barcelona
Barcelona, Spain