Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris
Primary Purpose
Postinflammatory Hyperpigmentation
Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Tranexamic Acid
Vehicle
Sponsored by
About this trial
This is an interventional treatment trial for Postinflammatory Hyperpigmentation focused on measuring Postinflammatory hyperpigmentation, Acne
Eligibility Criteria
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.
Sites / Locations
- WSUPG Dermatology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Right Side of Face
Left Side of Face
Arm Description
Patients will apply topical tranexamic acid to the dark spots on the one side of their face.
Patients will apply the vehicle cream without any medication to the dark spots on one side of their face.
Outcomes
Primary Outcome Measures
Change from Baseline Pigmentation at 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.
Change from Baseline Pigmentation at 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.
Change from Baseline Pigmentation at 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.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03361345
Brief Title
Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris
Official Title
Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of recruitment
Study Start Date
November 1, 2018 (Actual)
Primary Completion Date
January 9, 2022 (Actual)
Study Completion Date
January 9, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wayne State University
4. Oversight
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
Data Monitoring Committee
Yes
5. 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postinflammatory Hyperpigmentation
Keywords
Postinflammatory hyperpigmentation, Acne
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Right Side of Face
Arm Type
Experimental
Arm Description
Patients will apply topical tranexamic acid to the dark spots on the one side of their face.
Arm Title
Left Side of Face
Arm Type
Sham Comparator
Arm Description
Patients will apply the vehicle cream without any medication to the dark spots on one side of their face.
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Intervention Description
Topical tranexamic acid in cream form applied to dark spots on right side of face.
Intervention Type
Drug
Intervention Name(s)
Vehicle
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change from Baseline Pigmentation at 4 Weeks.
Description
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.
Time Frame
4 Weeks.
Title
Change from Baseline Pigmentation at 8 Weeks.
Description
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.
Time Frame
8 Weeks
Title
Change from Baseline Pigmentation at 12 Weeks.
Description
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.
Time Frame
12 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Daveluy
Organizational Affiliation
WSUPG Dermatology
Official's Role
Principal Investigator
Facility Information:
Facility Name
WSUPG Dermatology
City
Dearborn
State/Province
Michigan
ZIP/Postal Code
48124
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
20725554
Citation
Davis EC, Callender VD. Postinflammatory hyperpigmentation: a review of the epidemiology, clinical features, and treatment options in skin of color. J Clin Aesthet Dermatol. 2010 Jul;3(7):20-31.
Results Reference
background
PubMed Identifier
28670354
Citation
Darji K, Varade R, West D, Armbrecht ES, Guo MA. Psychosocial Impact of Postinflammatory Hyperpigmentation in Patients with Acne Vulgaris. J Clin Aesthet Dermatol. 2017 May;10(5):18-23. Epub 2017 May 1.
Results Reference
background
PubMed Identifier
28748406
Citation
Atefi N, Dalvand B, Ghassemi M, Mehran G, Heydarian A. Therapeutic Effects of Topical Tranexamic Acid in Comparison with Hydroquinone in Treatment of Women with Melasma. Dermatol Ther (Heidelb). 2017 Sep;7(3):417-424. doi: 10.1007/s13555-017-0195-0. Epub 2017 Jul 26.
Results Reference
background
PubMed Identifier
27135282
Citation
Kim SJ, Park JY, Shibata T, Fujiwara R, Kang HY. Efficacy and possible mechanisms of topical tranexamic acid in melasma. Clin Exp Dermatol. 2016 Jul;41(5):480-5. doi: 10.1111/ced.12835. Epub 2016 May 2.
Results Reference
background
PubMed Identifier
22329442
Citation
Na JI, Choi SY, Yang SH, Choi HR, Kang HY, Park KC. Effect of tranexamic acid on melasma: a clinical trial with histological evaluation. J Eur Acad Dermatol Venereol. 2013 Aug;27(8):1035-9. doi: 10.1111/j.1468-3083.2012.04464.x. Epub 2012 Feb 13.
Results Reference
background
PubMed Identifier
25422661
Citation
Ebrahimi B, Naeini FF. Topical tranexamic acid as a promising treatment for melasma. J Res Med Sci. 2014 Aug;19(8):753-7.
Results Reference
background
PubMed Identifier
24176524
Citation
Savory SA, Agim NG, Mao R, Peter S, Wang C, Maldonado G, Bearden Dietert J, Lieu TJ, Wang C, Pretzlaff K, Das S, Vandergriff T, Lopez IE, Litzner BR, Hynan LS, Arellano-Mendoza MI, Bergstresser PR, Pandya AG. Reliability assessment and validation of the postacne hyperpigmentation index (PAHPI), a new instrument to measure postinflammatory hyperpigmentation from acne vulgaris. J Am Acad Dermatol. 2014 Jan;70(1):108-14. doi: 10.1016/j.jaad.2013.09.017. Epub 2013 Oct 28.
Results Reference
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Topical 5% Tranexamic Acid as a Treatment for Postinflammatory Hyperpigmentation Due to Acne Vulgaris
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