Overview
Ultraviolet and UV-Visible Light Photoprotection for the Treatment of Melasma
Status:
Completed
Completed
Trial end date:
2013-11-01
2013-11-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Melasma is an acquired discoloration of the skin characterized by brown colour changes commonly on the face. The duration of this double-blind clinical trial will be 12 weeks. The control group will receive treatment with topical Hydroquinone (4%) and a Broad spectrum UV sunscreen. The experimental group, 4% topical hydroquinone and a Broad spectrum UV-visible light sunscreen. Visible light has melanotic properties and avoiding it can be part of the treatment for melasma patients. The estimated number of subjects to be recruited and randomized for the study is at least 25 per group. The purpose of this study is determine if there is a difference in the improvement between these two sunscreens types. Melasma Area and Severity Index (MASI) score will be assessed at the beginning of the study and at weeks 4, 8, and 12. Photographs, colorimetry and histological assessment will be also evaluated. Occurrence of adverse effects will also be recorded.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Universidad Autonoma de San Luis PotosíCollaborator:
Hospital Central "Dr. Ignacio Morones Prieto"Treatments:
Avobenzone
Benzophenone
Octylmethoxycinnamate
Oxybenzone
Sunscreening Agents
Terephthalylidene dicamphor sulfonic acid
Titanium dioxide
Zinc Oxide
Criteria
Inclusion Criteria:- Signed informed consent
- Women over 25 years of age
- Dermatologic diagnostic of melasma
- Phototype III or more
Exclusion Criteria:
- Pregnant or breastfeeding
- Postbirth, abortion in the past 6 months
- Having an endocrine or autoimmune disease
- Under hormonal therapy of any kind including contraceptives or it´s use in the past 6
months
- Currently under treatment for melasma including sunscreens
- Currently under radiation therapy, chemotherapy, immunosuppressants of any kind or
phototherapy or it´s use in the past 6 months
- Having used or are consuming photosensitizing substances, oral or topical