Simple drug may cut blood loss in breast surgery
NCT ID NCT05945680
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a single dose of tranexamic acid, given before surgery, can reduce blood loss in women undergoing breast cosmetic surgery. 60 women participated, and researchers measured blood loss, hemoglobin, and other clotting factors. The goal is to see if this common drug can make these procedures safer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- tranexamic acid
- What this could lead to
- If it works, this could offer a simple way to reduce bleeding during breast cosmetic surgery, potentially improving recovery.
- What could go wrong
- This is a small, completed phase 4 trial with only 60 participants. Results may not apply to all patients, and tranexamic acid carries a risk of blood clots.
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
-
60 people
The number who actually took part.
- Started
-
Sep 2023
- Finished
-
Sep 2025
- 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 to 75 years
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * women scheduled for breast esthetic surgery * ASA 1 or 2 * age \>18 and \<75 years Exclusion Criteria: * BMI \<20 or \>35 kg/m2 * ASA 3 or \> 3 * medical history of thromboembolism * history of hematological disease * treatment with aspirin 14 days before the procedure * treatment with anticoagulants 5 days before the procedure * epilepsy * allergy to tranexamic acid * coagulation disorders
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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
-
Poznan University of Medical Sciences
Poznan, Poland
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Other studies related to the condition(s) this trial covers.
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