Effect of TXA on Reducing Bruising After Filler Injection
University of Wisconsin, Madison · NCT06665594
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–89 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 2
- Target enrollment
- 40
- US sites recruiting
- 1
- Study start
- December 5, 2025
- Record last updated
- July 23, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this clinical trial is to look at the effect tranexamic acid (TXA) may have on reducing bruising, swelling, and pain after facial filler injection. The main question it aims to answer is:
- Does the addition of TXA to hyaluronic acid (HA) reduce bruising, swelling, and tenderness after HA injection?
Participants will receive the study medication along with the standard facial filler injection and complete surveys.
Being studied: Hyaluronic Acid (HA); Tranexamic Acid (TXA); Saline (placebo)
Conditions: Facial Filler Injections; Hyaluronic Acid; Tranexamic Acid
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Age equal to or greater than 18 but less than or equal to 89 years.
- Participants interested in facial filler (HA) injection.
- English speaking.
Exclusion Criteria
- Minors or under the age of 18
- Participant over the age of 89
- Pregnant or breast-feeding women
- Individuals unable to give consent due to another condition such as impaired decision-making capacity.
- Individuals with a history of a thrombotic event (DVT, PE, stroke, MI) or genetic disorder that increases risk of thrombosis
- Participants undergoing unilateral facial filler (HA) injection
- Participants with history of hypersensitivity to TXA or any of the other ingredients
- Participants that are on current therapeutic anticoagulation therapy and aspirin use
- Participants with stage 2 or greater renal failure
- Participants on hemodialysis or peritoneal dialysis
- History of diabetes or seizures
- Current tobacco smokers
- Acquired defective color vision
Recruiting US locations
University of Wisconsin - Madison
Madison, WI 53705
Site contact: Daniel Cho, MD, PhD · 608-263-7502 · chod@surgery.wisc.edu
Study contacts (from the official record)
- Daniel Cho, MD, PhD · 608-263-6330 · chod@surgery.wisc.edu
Similar studies in Wisconsin
All healthy volunteers studies in Wisconsin →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study to Learn How ASP3082 is Processed in Healthy Men
Astellas Pharma Global Development, Inc.
- Location
- Madison, WI
- Eligibility basics
- Ages 18–65 · Men only
- RecruitingHealthy volunteersPhase 1
A Trial of Lu AH69593 in Healthy Participants
H. Lundbeck A/S
- Location
- Madison, WI
- Eligibility basics
- Ages 18–55
- RecruitingHealthy volunteersPhase 1
Phase I Study to Assess the Safety and Efficacy of OCU200 for Center-Involved Diabetic Macular Edema (DME)
Ocugen
- Location
- La Crosse, WI + 4 other US sites
- Eligibility basics
- Ages 18+
- RecruitingHealthy volunteersPhase 1
A Trial to Compare the Pharmacokinetics of Two Presentations of Navenibart in Healthy Participants
Astria Therapeutics, Inc.
- Location
- Madison, WI + 2 other US sites
- Eligibility basics
- Ages 18–55