Beta Blocker De-prescription Following Coronary Artery Bypass Graft Surgery (BEEFBURGER Trial).
Launched by UNIVERSITY OF SASKATCHEWAN · Mar 6, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The BEEFBURGER Trial is a study looking at whether patients who have undergone coronary artery bypass graft (CABG) surgery still need to take beta-blockers, a type of medication that can help with heart issues. While beta-blockers are known to be very helpful for patients with weakened heart function or those at risk for certain heart problems, it’s not clear if they are still beneficial for patients without these risks after CABG surgery. This trial aims to gather more information about the long-term use of beta-blockers in these patients.
To participate in this trial, you need to be at least 18 years old and have had isolated CABG surgery. Additionally, you should still be taking beta-blockers at a follow-up appointment about 6 to 8 weeks after your surgery, and your heart function should be stable (with a certain level of heart strength measured recently). Participants can expect regular follow-up visits to track their health and how they respond to stopping or continuing beta-blocker therapy. The study is currently recruiting participants of all genders aged 65 and older. If you have any questions about your eligibility or the trial itself, it's a good idea to talk to your healthcare provider.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age ≥ 18 years treated with index isolated CABG
- • Able to consent to study
- • On beta blocker therapy at the 6-8week visit
- • LV systolic function (≥45% assessed within 6months of CABG date)
- Exclusion Criteria:
- • Prior heart failure with reduced ejection fraction (LVEF \<45%)
- • Pre- or peri-operative atrial fibrillation or flutter
- • Peri-CABG stroke
- • Unable to follow-up
About University Of Saskatchewan
The University of Saskatchewan is a leading research institution dedicated to advancing health sciences through innovative clinical trials and studies. With a commitment to improving patient outcomes, the university leverages its interdisciplinary expertise and state-of-the-art facilities to conduct rigorous and ethically sound research. By fostering collaborations among researchers, healthcare professionals, and industry partners, the University of Saskatchewan aims to translate scientific discoveries into practical applications that enhance healthcare delivery and contribute to the well-being of communities both locally and globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Saskatoon, Saskatchewan, Canada
Patients applied
Trial Officials
Haissam Haddad, MD, FRCPC
Study Chair
University of Saskatchewan
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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