RECRUITING

Perioperative Anticoagulant Use for Surgery Evaluation -Virtual Visit (PAUSE-Virtual)

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 purpose of the PAUSE-Virtual Study is to show that by changing pre-surgery visits with patients taking a blood thinner (direct oral anticoagulant (apixaban, dabigatran, edoxaban, rivaroxaban or warfarin) when the participant requires elective surgery, using a standard, in-person proven approach, to a virtual visit, either telephone or video conference, is as safe. Patients who are receiving a blood thinner for the medical condition known as atrial fibrillation (AF) and require an elective surgery/procedure, is common. These patients have to stop taking their blood thinner for a certain time before the procedure to reduce serious complications of stroke or bleeding. For doctors who help manage these patients before a procedure, appointments have been traditionally done in-person. Patients receive instructions about when to stop and restart their blood thinners and taught how to self-administrator a short acting blood thinner (heparin) if needed. The COVID pandemic changed the way these appointments were done, making it important to contact these patients without them having to come to the hospital for an in person visit. Virtual patient care, by telephone or video conference, to communicate to patients about when to start and restart their blood thinner was necessary. This study wants to show that this virtual method of instruction, using a standardized plan of managing patient care, is easy, acceptable to patients and as safe when compared to an in-person meeting. Such instruction would also be cost-efficient standard post-pandemic. Prior work has shown that both a standard care of patients who are receiving blood thinners and a point-of-care decision "app", available through Thrombosis Canada (www.thrombosiscanada.ca) website, have been trusted during this virtual visit successfully. The investigator will show, by following up at 30 days, that this standardized management plan is safe and can be done virtually, with a low risk of stroke and major bleeding.

Official Title

Perioperative Anticoagulant Use for Surgery Evaluation -Virtual Visit (PAUSE-Virtual), a Simple Perioperative Anticoagulant Management Approach, Replacing a Resource-intensive In-person Doctor-patient Consultation, with a Simple Virtual Care Model That Will Provide a New Standard of Care for Patients on a Direct Oral Anticoagulant or Warfarin and Require Elective Surgery/procedure.

Quick Facts

Study Start:2021-12-01
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06844227

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:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 years of age or older with AF/flutter (chronic, persistent, paroxysmal) that requires anticoagulation
  2. * Receiving warfarin, with a target international normalized ratio (INR) range of 2.0-3.0, or a DOAC, comprising one of the following regimens: apixaban, 2.5 mg or 5 mg bid; edoxaban, 30 mg or 60 mg daily; dabigatran, 110 mg or 150 mg bid; or rivaroxaban, 15 mg or 20 mg daily
  3. * Require an elective (planned, non-urgent) surgery or invasive medical or surgical procedure
  1. * Indication for anticoagulation is not AF/flutter (e.g., mechanical heart valve, VTE, other)
  2. * Non-standard anticoagulant regimen used (e.g., warfarin INR 3-4, rivaroxaban 2.5 mg bid)
  3. * In DOAC users only: creatinine clearance \<25 mL/min (that preclude DOAC use)
  4. * Cognitive impairment or psychiatric illness (that precludes reliable contact during follow-up)
  5. * Unable or unwilling to provide consent for virtual care (in-person care will be provided)
  6. * Previous participation in this study for an elective surgery/procedure

Contacts and Locations

Study Contact

James D Douketis, MD
CONTACT
905-522-1155
jdouket@mcmaster.ca
Melanie St John
CONTACT
905-525-9140
stjohm1@mcmaster.ca

Principal Investigator

James D Douketis, MD
PRINCIPAL_INVESTIGATOR
McMaster University/St. Joseph's Healthcare

Study Locations (Sites)

Endeavor Health - Northshore
Evanston, Illinois, 60201
United States
Henry Ford
Detroit, Michigan, 482032
United States
Northwell Health
Great Neck, New York, 11021
United States
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, 19107
United States

Collaborators and Investigators

Sponsor: McMaster University

  • James D Douketis, MD, PRINCIPAL_INVESTIGATOR, McMaster University/St. Joseph's Healthcare

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 Date2021-12-01
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2021-12-01
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • anticoagulation
  • Atrial Fibrillation
  • Surgery
  • Oral Anticoagulant
  • Blood Thinner
  • DOAC
  • Interruption
  • Perioperative
  • Virtual
  • PAUSE

Additional Relevant MeSH Terms

  • Atrial Fibrillation (AF)