Melasma Clinical Trial
Official title:
Combined Trichlotoaceticacid and Microneedle Versus Trichlroacetic Acid Alone in the Treatment of Melasma
Verified date | February 2018 |
Source | Assiut University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Melasma is an acquired disorder of hyperpigmentation characterised by blotchy, light-to-dark
brown macules distributed symmetrically on the sun-exposed parts of the body.
Although many factors have been proposed to have a role in pathogenesis, the exact ethology
is yet to be understood. The most commonly identifiable risk factors include ultraviolet
radiation, genetic predisposition, pregnancy, oral contraceptives, thyroid disease and drugs
like antiepileptic. The excessive pigmentation has been attributed to both melanocytosis
(increased number of melanocytes) as well as melano genesis (excess production of melanin) as
confirmed in a histopathological study on Asian patients.] Furthermore, a vascular component
has also been proposed to play a role in the pathogenesis of melisma. Kim et al. have found
that lesion melasma skin had greater expression of the vascular endothelial growth factor in
keratinocytes compared to nearby nonlesional skin.
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | April 5, 2020 |
Est. primary completion date | April 5, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Both sex will be included Age range from 18- 50 yrs.' old Patients with realistic expectations. Exclusion Criteria: - patients taking oral contraceptive pills. patients with history of polycystic ovary. pregnant and lactating females. patients with active infection. patients on isotretinoin. patients with history of keloids,or hypertrophic scars. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Assiut University |
Sheth VM, Pandya AG. Melasma: a comprehensive update: part II. J Am Acad Dermatol. 2011 Oct;65(4):699-714; quiz 715. doi: 10.1016/j.jaad.2011.06.001. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Scoring of the patients according to modified melasma are abd severity index [mMASI] Scoring before and After last session will be done by 1 month | Efficacy of the treatment =(mMASIscorebefor -mMASIscoreafter)/mMASIscore before x100. Clinical efficacy was categorized into : Excellent response: if morethan 75%fall in [mMASI] score. Very good response:if 50-75%fall in ]mMASI[score . Good respone: if 25-50%fall in ]mMASI[score. Poor response: if less25%fall in mMASIscore. No response: when there was no change in [mMASI] score at the end of the therapy. Efficacy of the treatment =(mMASIscorebefor -mMASIscoreafter)/mMASIscore before x100. Clinical efficacy was categorized into : Excellent response: if morethan 75%fall in [mMASI] score. Very goodresponse:if 50-75%fall in ]mMASI[score . Good respone: if 25-50%fall in ]mMASI[score. Poor response: if less25%fall in mMASIscore. No response: when there was no change in [mMASI] score at the end of the therapy. |
1 month after last session | |
Primary | [mMASI] Scoring before and After last session will be done by 3 months | before x100. Clinical efficacy was categorized into : Excellent response: if morethan 75%fall in [mMASI] score. Very good response:if 50-75%fall in ]mMASI[score . Good respone: if 25-50%fall in ]mMASI[score. Poor response: if less25%fall in mMASIscore. No response: when there was no change in [mMASI] score at the end of the therapy. Efficacy of the treatment =(mMASIscorebefor -mMASIscoreafter)/mMASIscore before x100. Clinical efficacy was categorized into : Excellent response: if morethan 75%fall in [mMASI] score. Very goodresponse:if 50-75%fall in ]mMASI[score . Good respone: if 25-50%fall in ]mMASI[score. Poor response: if less25%fall in mMASIscore. No response: when there was no c |
3 months after last session |
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