Tranexamic Acid for Nasal Mohs Reconstruction

This study is looking at whether a medication called tranexamic acid (TXA) can help reduce swelling and bruising after nasal reconstruction surgery. This surgery often happens after Mohs surgery for skin cancer on the face. You would receive an injection of either tranexamic acid mixed with a local anesthetic (1% lidocaine with 1:100,000 epinephrine) or just the local anesthetic. Researchers want to see if tranexamic acid, which helps blood clot, can improve how your surgical site looks and feels. To join, you must be at least 18 years old and having a specific type of nasal reconstruction surgery (local flap) at Vanderbilt University Medical Center. The study will measure swelling and bruising one week after surgery, and bleeding during surgery. The current recruitment status is unclear.

Study design
This is a randomized controlled trial planning to enroll 100 participants. Participants will be randomly assigned to receive either the treatment or the control injection.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your surgical site swelling and bruising will be measured one week after surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06057675

Tranexamic Acid in Nasal Mohs Reconstruction

Recruiting
PHASE2Ages 18+InterventionalPrevention
Vanderbilt University Medical Center
~100 participants
Updated 2026-09-09 on ClinicalTrials.gov
What's tested:Treatment (tranexamic acid and 1% lidocaine with 1:100,000 epinephrine)Control (1% lidocaine with 1:100,000 epinephrine)

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Surgical site swelling and bruising (surgeon)
Measured over One week
+3 more outcomes measured
Postoperative Bleeding
Skin Cancer Face

NCT06057675

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Vanderbilt University Medical Center

    Nashville, Tennesseeno site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Priyesh Patel, MD · PRINCIPAL_INVESTIGATOR · Vanderbilt University Medical Center

Opens a ready-to-send draft in your own email app — review before sending.

  • Surgical site swelling and bruising (surgeon)One week

    Photos will be taken by a research team member at the first postoperative clinic visit and then analyzed and graded by a blinded reviewer for measures including surgical site bruising and swelling. Surgical site swelling and bruising will be graded on a 4 point scale, with 0 indicating no swelling and bruising and 3 indicating significant swelling and bruising.

  • Surgical site swelling and bruising (patient)One week

    Subjective measures of patient perceived swelling and bruising will be collected via a patient completed survey given at the first postoperative clinic visit. Surgical site swelling and bruising will be graded on a 4 point scale, with 0 indicating no swelling and bruising and 3 indicating significant swelling and bruising.

  • Intraoperative bleedingIntraoperative

    Intraoperative bleeding will be assessed using the validated Boezaart Bleeding scale (6 point scale, with 0 indicating no bleeding/cadaveric conditions and 5 indicating severe bleeding/constant suctioning required). Values will be assigned by the attending surgeon and recorded by the research team.

  • Intraoperative bleedingIntraoperative

    Attending surgeon will score the approximate percent blood saturation of each surgical sponge used in the case. Values from each sponge will be added together for a total cumulative value, with a higher cumulative value indicating a greater amount of intraoperative bleeding.