RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2021-11-17
Study Completion:2026-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04973397

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 45-64 years of age with at least one risk factor, or ≥65 years of age;
  2. * undergoing elective noncardiac same-day surgery;
  3. * planned duration in the operating room 60 minutes or more;
  4. * provided written consent.
  1. * intervention does not require the presence of an anesthesiologist;
  2. * procedure is performed by a nonsurgical specialty (e.g., gastroenterology, pneumology, radio-oncology or radiology);
  3. * intervention is an ophthalmologic procedure;
  4. * previously enrolled in the VALIANCE study.

Contacts and Locations

Study Contact

Melodie Fanay Boko, MSc
CONTACT
514-890-8000
melodie.fanay.boko.chum@ssss.gouv.qc.ca

Principal Investigator

Emmanuelle Duceppe, MD, PhD
PRINCIPAL_INVESTIGATOR
Centre Hospitalier de l'Universite de Montreal (CHUM)

Study Locations (Sites)

Wake Forest Baptist Medical Centre
Winston-Salem, North Carolina, 27157
United States
Cleveland Clinic Foundation Fairview Campus
Cleveland, Ohio, 44111
United States
Cleveland Clinic Foundation Main Campus
Cleveland, Ohio, 44195
United States

Collaborators and Investigators

Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)

  • Emmanuelle Duceppe, MD, PhD, PRINCIPAL_INVESTIGATOR, Centre Hospitalier de l'Universite de Montreal (CHUM)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-11-17
Study Completion Date2026-08

Study Record Updates

Study Start Date2021-11-17
Study Completion Date2026-08

Terms related to this study

Keywords Provided by Researchers

  • Preoperative Care
  • Surgery
  • Postoperative complications
  • Same-day surgery
  • Ambulatory surgery
  • Outpatient surgery

Additional Relevant MeSH Terms

  • Preoperative Care
  • Surgery--Complications
  • Myocardial Infarction