Reversal of Atrial Substrate to Prevent Atrial

NCT03682991 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 509

Last updated 2026-02-17

No results posted yet for this study

Summary

A multi-center, randomized trial to examine the effect of aggressive risk factor control and arrhythmia trigger-based intervention on recurrence of atrial fibrillation.

Conditions

Interventions

OTHER

Aggressive Risk Factor Control

1. Sleep apnea screening, therapy is recommended if apopnea-hypopnea (AHI) index is greater than 15, with a target index of less than 5. 2. Counseling regarding alcohol reduction to 2 drinks/day for men, 1 drink/day for women, no binge drinking (\>5 drinks at one setting). 3. Participation in a 12 week structured, home-based exercise program and nutritional counseling. Weight reduction will be emphasized through modification of diet and exercise. 4. Blood Pressure management to achieve a target systolic blood pressure (SBP) of \<120/80 mm/Hg 5. Smoking cessation facilitated through local resources already established at each site

OTHER

Standard of Care

Recommendations based on current guidelines

Sponsors & Collaborators

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • Abbott

    collaborator INDUSTRY
  • Philips Healthcare

    collaborator INDUSTRY
  • Cardiac Arrhythmia Network of Canada

    collaborator OTHER
  • Nova Scotia Health Authority

    lead OTHER

Principal Investigators

  • John Sapp · Nova Scotia Health Authority

  • Isabelle vanGelder · University of Groningen

  • Ratika Parkash · Nova Scotia Health Authority

  • Allan Skanes · London Health Sciences Centre

  • Chris Blanchard · Nova Scotia Health

  • David Birnie · University of Ottawa Heart Institution

  • George Wells · University of Ottawa Heart Institution

  • Michiel Rienstra · University of Groningen

  • Jeff Healey · Hamilton Health Sciences Centre

  • Jennifer Reed · University of Ottawa Heart Institution

  • Anthony Tang · London Health Sciences Centre

  • Vidal Essebag · McGill University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-01
Primary Completion
2027-09-15
Completion
2027-12-31

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03682991 on ClinicalTrials.gov