Optimal Cardiopulmonary Bypass and Anticoagulation Management Strategies in Obese Patients Undergoing Cardiac Surgery

Recruiting N/A Interventional Study
Cardiopulmonary Bypass Obesity
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
410 (estimated)
Sponsor
Laval University · Other
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About This Trial

Standard Heparin management, based on total body weight, is not well established for obese patients undergoing cardiac surgery with cardiopulmonary bypass (CPB). The purpose of this study is to assess the safety and efficacy of using lean body mass (LBM) to determine pump flow rate and/or Heparin dosage in obese patients undergoing CPB.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Obese patients (BMI ≥ 30kg/m2) * Planned cardiac surgery * Age ≥ 18 years Exclusion Criteria: * Permanent pacemaker * Known intolerance to protamine * Known or suspected allergy to the used antifibrinolytic agent * Refusal to receive blood products * Planned off pump coronar…
Contacts

Hugo Tremblay, Bachelor

418-656-8711

hugo.tremblay@criucpq.ulaval.ca

CONTACT