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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00166192
Other study ID # IRB00024850
Secondary ID
Status Completed
Phase Phase 4
First received September 13, 2005
Last updated November 12, 2013
Start date January 2008
Est. completion date November 2013

Study information

Verified date November 2013
Source Emory University
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Melasma is an acquired discoloration of the skin characterized by brown patches. Chemical peels using agents such as Jessner's solution and trichloroacetic acid (TCA) are commonly used to treat melasma. A chemical peel involves applying the peeling agent to the skin for a short period. The skin will peel similar to a sunburn, and moisturizers are applied to the skin. Although both agents are well-accepted, there have been no good comparisons of the two agents. The purpose of this study is determine if there is a difference in the effectiveness of these two agents.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date November 2013
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults > 18 years old

- Clinical diagnosis of melasma

- Mental capacity to give informed consent

Exclusion Criteria:

- Pregnancy

- H/o allergy to Jessner's solution, tricholoracetetic acid, tretinoin, or hydroquinone

- Active dermatitis

- Presence of cutaneous infection

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Jessner's solution chemical peel

Trichloroacetic acid chemical peel


Locations

Country Name City State
United States Emory University Dermatology Clinic Atlanta Georgia

Sponsors (1)

Lead Sponsor Collaborator
Emory University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical efficacy by clinician's evaluation Hyperpigmenation Global Score 3 months No
Secondary Efficacy by subject's evaluation Hyperpigmentation Global Score 3 months No
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