Can a clotting drug cut mastectomy wound drainage?
NCT ID NCT07800832
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether applying tranexamic acid directly to the wound during a mastectomy reduces the amount and duration of fluid drainage afterward. Researchers will compare 30 patients who receive the topical drug with 30 who get standard postoperative care. The goal is to see if this simple addition can speed up recovery and lower the risk of wound infection.
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 applied directly to the surgical wound
- What this could lead to
- If it works, this could offer a simple way to reduce wound drainage after mastectomy, potentially leading to faster recovery and fewer complications.
- What could go wrong
- This is a small, early-stage trial, so results may not apply broadly. Tranexamic acid can increase clotting risk, though the trial excludes people with a history of blood clots or clotting disorders.
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
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
60 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Mar 2026
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1\. All patients diagnosed with ductal or lobular breast carcinoma for whom MRM is indicated. Exclusion Criteria: 1. History of thromboembolic events. 2. Patients with coagulation disorders. 3. Currently on anticoagulant therapy.
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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
-
Gulab Devi Educational
Lahore, Punjab Province, Pakistan
-
Gulab Devi hospital
Lahore, Punjab Province, Pakistan
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