Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT04233749

The Efficacy of Tranexamic Acid in the Treatment of Lichen Planus Pigmentosus and Erythema Dyschromicum Perstans

Led by Henry Ford Health System · Updated on 2025-09-09

5

Participants Needed

1

Research Sites

302 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

There are currently no effective treatments for lichen planus pigmentosus (LPP) and erythema dyschromicum perstans (EDP). Tranexamic acid, which may downregulate pigmentation through a reduction in plasmin, has been shown to decrease pigmentation in patients with melasma, another pigmentary disorder. Given that LPP, EDP, and melasma are all disorders of pigmentation with dermal involvement, it is possible that tranexamic acid can also reduce pigmentation in LPP and EDP as well.

CONDITIONS

Official Title

The Efficacy of Tranexamic Acid in the Treatment of Lichen Planus Pigmentosus and Erythema Dyschromicum Perstans

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis of lichen planus pigmentosus, erythema dyschromicum perstans, or ashy dermatosis
  • Able to understand the study requirements and risks
  • Able to sign a consent form
  • Discontinued all topical or oral pigmentation treatments except sunscreen at least one month before treatment
Not Eligible

You will not qualify if you...

  • Personal history of clotting disorders or thromboembolic diseases (e.g., deep vein thrombosis, stroke)
  • Active cancer, excluding non-melanoma skin cancer
  • Moderate to severe kidney impairment
  • History of migraine with aura
  • Current use of anticoagulant medications
  • Use of hormonal contraception or hormone replacement therapy within the past 30 days
  • Women who are lactating, pregnant, or planning pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

New Center One

Detroit, Michigan, United States, 48202

Actively Recruiting

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Research Team

A

Angela Parks-Miller, RN

CONTACT

J

Jennifer Creasor, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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