Rapid Recovery Pathway for Heart Bypass Surgery

Study to Evaluate the Impact of the Recovery Pathway on Postoperative Leght of Stay in Coronary Artery Bypass Surgery

Recruiting N/A Interventional Study
Enhanced Recovery After Surgery Quality Improvement
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
128 (estimated)
Sponsor
University of Sao Paulo General Hospital · Other
Who this trial is looking for

This trial is looking for adult patients who will have heart bypass surgery. Participants will either follow a quick recovery plan or the usual care plan after their surgery.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am an adult over 18 years old
  • I will have isolated coronary artery bypass surgery
  • I can provide signed consent to join the trial

You may not be able to join if

  • I am having emergency surgery
  • I have severe heart dysfunction
  • I have kidney problems
  • I have atrial fibrillation or need blood thinners
  • I have moderate to severe anemia
  • I have a high STS risk score over 4%
  • I or my family do not agree with the study
  • I cannot sign the informed consent form

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
This randomized and prospective trial aims to evaluate the implementation of a rapid recovery protocol for coronary artery bypass grafting (CABG) in a hospital serving patients from the Brazilian Unified Health System (Sistema Único de Saúde - SUS). The study will compare outcomes between two groups: patients receiving care under the rapid recovery protocol and those following the standard institu…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult patients (\>18 years old) * Undergoing isolated coronary artery bypass grafting (CABG) with elective or urgent status * Signed informed consent form (ICF) Exclusion Criteria: * Emergency patients * Severe ventricular dysfunction (ejection fraction \<30%) * Renal impair…
Contacts

Omar A V Mejia, md, PhD

555+(11) 2661-5014

omarvmejia@gmail.com

CONTACT