Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris

Sponsor
Wayne State University (Other)
Overall Status
Terminated
CT.gov ID
NCT03361345
Collaborator
(none)
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Study Details

Study Description

Brief Summary

The goal of this study is to determine if topical tranexamic acid is capable of decreasing the pigment of the dark spots left from acne bumps. The first line medication used for this often is not tolerated well by patients, and topical tranexamic acid has minimal reported side effects thus far.

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Split-face study in which topical tranexamic acid will be applied to one side of the face and the other side of the face will be the placebo/vehicle as a control.Split-face study in which topical tranexamic acid will be applied to one side of the face and the other side of the face will be the placebo/vehicle as a control.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris
Actual Study Start Date :
Nov 1, 2018
Actual Primary Completion Date :
Jan 9, 2022
Actual Study Completion Date :
Jan 9, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Right Side of Face

Patients will apply topical tranexamic acid to the dark spots on the one side of their face.

Drug: Tranexamic Acid
Topical tranexamic acid in cream form applied to dark spots on right side of face.

Sham Comparator: Left Side of Face

Patients will apply the vehicle cream without any medication to the dark spots on one side of their face.

Drug: Vehicle
The Vehicle is going to be a cream without any active medication that will be applied as a control substance for the topical tranexamic acid cream, and will be applied to the contralateral side of the face.

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline Pigmentation at 4 Weeks. [4 Weeks.]

    Patients will have their lesion pigmentation scored with the postacne hyperpigmentation index after 4 weeks. The postacne hyperpigmentation index (PAHPI) assesses hyperpigmentation lesions after acne based on the median lesion size, the median lesion intensity, and the number of lesions present. The total score can range from 6-22 points. Subscales will measure lesion size, lesion intensity, and number of lesions. Subscales will be assigned a number based on the table in the protocol, and then added together to form the total score. Higher values indicate worse hyperpigmentation. We will measure the total decrease in the PAHPI at the follow-up visit.

  2. Change from Baseline Pigmentation at 8 Weeks. [8 Weeks]

    Patients will have their lesion pigmentation scored with the postacne hyperpigmentation index after 8 weeks. The postacne hyperpigmentation index (PAHPI) assesses hyperpigmentation lesions after acne based on the median lesion size, the median lesion intensity, and the number of lesions present. The total score can range from 6-22 points. Subscales will measure lesion size, lesion intensity, and number of lesions. Subscales will be assigned a number based on the table in the protocol, and then added together to form the total score. Higher values indicate worse hyperpigmentation. We will measure the total decrease in the PAHPI at the follow-up visit.

  3. Change from Baseline Pigmentation at 12 Weeks. [12 Weeks]

    Patients will have their lesion pigmentation scored with the postacne hyperpigmentation index after 12 weeks. The postacne hyperpigmentation index (PAHPI) assesses hyperpigmentation lesions after acne based on the median lesion size, the median lesion intensity, and the number of lesions present. The total score can range from 6-22 points. Subscales will measure lesion size, lesion intensity, and number of lesions. Subscales will be assigned a number based on the table in the protocol, and then added together to form the total score. Higher values indicate worse hyperpigmentation. We will measure the total decrease in the PAHPI at the follow-up visit.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 18 to 65

  • Patients with bilateral involvement of facial postinflammatory hyperpigmentation due to acne vulgaris.

Exclusion Criteria:
  • Pregnant patients or patients planning to become pregnant during the time of the study.

  • Patients with a history of use of hydroquinone, kojic acid, tretinoin, adapalene, tazarotene or azaleic acid in the previous 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 WSUPG Dermatology Dearborn Michigan United States 48124

Sponsors and Collaborators

  • Wayne State University

Investigators

  • Principal Investigator: Steven Daveluy, WSUPG Dermatology

Study Documents (Full-Text)

More Information

Publications

Responsible Party:
Steven D Daveluy, Program Director of Wayne State University Department of Dermatology, Wayne State University
ClinicalTrials.gov Identifier:
NCT03361345
Other Study ID Numbers:
  • 1709000866
First Posted:
Dec 4, 2017
Last Update Posted:
May 4, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Steven D Daveluy, Program Director of Wayne State University Department of Dermatology, Wayne State University
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 4, 2022