dc.contributor.author |
Orlandi-Jorquera, Cecilia |
|
dc.contributor.author |
Moran-Cardenas, María Gabriela |
|
dc.contributor.author |
Escobar-Huenchul, Valery Magdalena |
|
dc.date.accessioned |
2019-06-24T22:33:02Z |
|
dc.date.available |
2019-06-24T22:33:02Z |
|
dc.date.issued |
2016 |
|
dc.identifier.citation |
ORLANDI-JORQUERA, Cecilia, MORAN-CARDENAS, María Gabriela, ESCOBAR-HUENCHUL, Valery Magdalena. Comparative clinical study of depigmentation products on facial melasma in Latin women. In: Curierul Medical. 2016, vol. 59, no 4, pp. 29-32. ISSN 1875-0666. |
|
dc.identifier.issn |
1857-0666 |
|
dc.identifier.uri |
http://moldmedjournal.md/wp-content/uploads/2016/09/Cm-4-2016-PDF.pdf |
|
dc.identifier.uri |
http://repository.usmf.md/handle/20.500.12710/2933 |
|
dc.description.abstract |
Background: Hyperpigmented lesions need the most frequent dermatological consultations, the acquired ones being more effectively treated. Out of
them, the most common is melasma, which is currently treated with hydroquinone. Our objective was to compare the efficacy of a treatment based on
Diacetylboldine-DAB, Alpha arbutin and Licorice with hydroquinone 4%.
Material and methods: We carried out a pilot study on 30 Latin patients (skin type III and IV after Fitzpatrick’s classification). The product under study
was applied on one side of the face and hydroquinone on the other, during 60 days.
Results: The study product demonstrated effectiveness comparable to 4% hydroquinone in the 60 days of monitoring time. The hyperpigmentations are
of a chronic type and so, considering the formula of the study product, it has the great advantage of permitting use for a prolonged period of time without
the risk of undesirable side effects such as ochronosis. Tolerance for the product was excellent as well, both for daytime and night-time formulations,
and neither irritation reactions nor allergic reactions were present during the period of use.
Conclusions: The combined use of active substances is similar and comparable to hydroquinone in a 60 day period. The foundation can be laid for
future studies to approach a new investigation with a larger number of patients, in which the use of hydroquinone can be established in comparison with
this new treatment, so as to allow a statistically significant relationship to be established. Additionally, by studying a larger number of participants, it
would allow this new product to be set up as an effective alternative treatment for melasma. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Ministerul Sănătăţii al Republicii Moldova, Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” |
en_US |
dc.relation.ispartof |
Curierul Medical |
|
dc.subject |
facial melasma |
en_US |
dc.subject |
antipigment skin agents |
en_US |
dc.subject.mesh |
Melanosis--drug therapy |
en_US |
dc.subject.mesh |
Facial Dermatoses--drug therapy |
en_US |
dc.subject.mesh |
Skin Pigmentation--drug effects |
en_US |
dc.subject.mesh |
Hydroquinones--therapeutic use |
en_US |
dc.title |
Comparative clinical study of depigmentation products on facial melasma in Latin women |
en_US |
dc.type |
Article |
en_US |