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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00616239
Other study ID # 082007-078
Secondary ID IRB File 082007-
Status Completed
Phase Phase 4
First received
Last updated
Start date January 2008
Est. completion date March 2018

Study information

Verified date July 2020
Source University of Texas Southwestern Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will enroll 20 adult Hispanic women. Participants will apply 4% hydroquinone cream twice daily to affected areas on the face for 14 weeks and half the face will be peeled with 20-30% salicylic acid every two weeks for a total of 4 peels. The first two peels will be 20% salicylic acid and the second two peels will be with 30% salicylic acid. The purpose of the study will be to evaluate the safety and efficacy of salicylic acid combined with 4% hydroquinone versus 4% hydroquinone alone.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Hispanic women ages 18-65 years of age with moderate to severe melasma

- English and Spanish-speaking women

Exclusion Criteria:

- Pregnant or breast-feeding women

- Subjects who have used 4% hydroquinone within 3 months of study start

- Subjects who have used chemical peels, microdermabrasion or facial laser treatments within 9 months of study start

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
20-30% Salicylic Acid peels to the right side of the face
Two 20% salicylic acid peels two weeks apart followed by 2 30% salicylic acid peels two weeks apart to the right side of the face.
20-30% Salicylic Acid peels to the left side of the face
Two 20% salicylic acid peels two weeks apart followed by 2 30% salicylic acid peels two weeks apart to the left side of the face

Locations

Country Name City State
United States UT Southwestern Medical Center at Dallas - Dermatology Clinical Trials Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants Showing Improvement of Melasma Based on Mexameter Readings Improvement of melasma on the peel side using mexameter reading 14 weeks
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