New heparin dosing for obese heart surgery patients may cut bleeding risk
NCT ID NCT02675647
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using ideal body weight (instead of total body weight) to calculate heparin doses during heart-lung bypass reduces excessive bleeding in obese patients. Sixty obese adults scheduled for heart surgery were randomly assigned to receive heparin based on either ideal or total body weight. Researchers measured heparin levels, clotting time, bleeding, and transfusion needs to see if the new dosing is safer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Heparin
- What this could lead to
- If successful, this could lead to safer heparin dosing guidelines for obese patients undergoing heart surgery, reducing bleeding risks.
- What could go wrong
- This is a small, single-center Phase 4 study with only 60 participants, so results may not apply broadly. The approach may not significantly reduce bleeding or complications.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Dec 2015
- Finished
-
Dec 2017
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Obese patients (BMI ≥ 30 kg/m²) * Planned cardiac surgery under cardiopulmonary bypass * Coronary-artery bypass graft, or valve surgery) * Age ≥ 18 yo Exclusion criteria: * Allergy to heparin * Emergency surgical intervention * Redo surgery * Heart transplantation * Surgery for circulatory assistance * Pre-operative heparin use
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Hôpitaux Universitaires de Strasbourg
Strasbourg, 67091, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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