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CompletedNCT01092884

Polypodium Leucotomos Extract for the Treatment of Melasma

Polypodium Leucotomos Extract as an Adjunct to Sunscreen for the Treatment of Melasma

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of Texas Southwestern Medical Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

We will assess whether oral supplementation with Polypodium leucotomos, a commercially marketed fern extract, improves facial melasma in Hispanic women with moderate to severe melasma. Subjects will be randomized to either Group 1, which will receive oral Polypodium leucotomos extract plus topical sunscreen, or Group 2, which will receive oral placebo plus topical sunscreen. The study will last 12 weeks, and we hypothesize that the Polypodium leucotomos group will have more improvement in their melasma compared to the placebo group.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPolypodium leucotomos extract240 mg capsule of Polypodium leucotomos extract will be taken orally three times daily
OTHERPlaceboThis placebo capsule will be taken orally three times daily

Timeline

Start date
2010-03-01
Primary completion
2011-07-01
Completion
2012-07-01
First posted
2010-03-25
Last updated
2023-09-06

Source: ClinicalTrials.gov record NCT01092884. Inclusion in this directory is not an endorsement.

Polypodium Leucotomos Extract for the Treatment of Melasma (NCT01092884) · Clinical Trials Directory