Silymarin Cream Versus Combined Silymarin Cream and Microneedling in Treatment of Melasma

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05099601
Collaborator
(none)
30
1
7

Study Details

Study Description

Brief Summary

Melasma is an acquired pigmentary disorder, occurring most commonly on the face. It is more prevalent in females and darker skin types. Melasma is mainly a clinical diagnosis consisting of symmetric reticulated hypermelanosis in three predominant facial patterns: centrofacial, malar, and mandibular. Melasma, though benign, can be extremely psychologically distressing and has been shown to have a significant impact on quality of life, social and emotional wellbeing. Multiple factors are implicated in the pathogenesis of melasma; however, the definite underlying mechanisms are not yet completely established. Ultraviolet exposure is one of the leading etiological factors, besides genetic and hormonal factors.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: Silymarin
  • Procedure: Microneedling
Phase 4

Detailed Description

Many studies examined multiple treatment options for melasma, but none of them is completely satisfactory with recurrence in most cases.

Silymarin (SM) is a standardized extract from Silybum marianum seeds, is traditionally used as a hepatoprotective agent for its potent regenerative properties. Lately, SM is utilized in dermatological and cosmetic preparations for its antioxidant effect, anti-inflammatory and immunomodulatory properties.

Silibinin, the main component of silymarin, has been found to have antioxidant properties. It decreases the hazardous effects of solar ultraviolet radiation and significantly prevents melanin production in a dose-dependent manner without effect on cell viability.

Skin microneedling, or percutaneous collagen induction by needles, is a minimally invasive procedure that uses short fine needles to puncture the skin and stimulates fibroblast proliferation, release of growth factors and collagen production.

Long-term improvement of melasma after microneedling was reported , however, the exact mechanism that promotes skin lightening is not known.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Each side of the patients' face will be randomly allocated to either topical silymarin 0.7% and microneedling or topical silymarin 0.7% alone.Each side of the patients' face will be randomly allocated to either topical silymarin 0.7% and microneedling or topical silymarin 0.7% alone.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Topical Silymarin Versus Combined Topical Silymarin and Microneedling in Treatment of Melasma: Split Face Study
Anticipated Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Silymarin alone versus silymarin and microneedling

There will be one group of patients. Each side of the patients' face will be randomly allocated to either topical silymarin 0.7% and microneedling or topical silymarin 0.7% alone.

Combination Product: Silymarin
The patients will use topical silymarin 0.7% cream on the face twice daily(home use).

Procedure: Microneedling
Patients will be subjected to microneedling sessions on one side of the face. Three consecutive sessions, 4 weeks apart (0, 4, 8 weeks), will be performed by dermapen. Sessions will be done by well trained physician.

Outcome Measures

Primary Outcome Measures

  1. compare between the efficacy of topical silymarin alone and its combination with microneedling in treatment of melasma. [3 months]

    Scoring of the patients according to modified Melasma Area and Severity Index (mMASI) score before and after treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age: 18-50 years old.

  • Pattern of melasma: Bilateral symmetrical facial melasma of any pattern.

  • Fitzpatrick skin phototypes: Types III, IV and V

Exclusion Criteria:
  • Pregnancy and lactation.

  • Patients taking oral contraceptive pills, hormonal replacement therapy or treatment for chronic illness at the time of the study or during the past 6 months.

  • Coexistance of diseases associated with hyperpigmentation such as Addison disease.

  • Scarring and keloid tendency, active skin infections as active HSV.

  • Previous history of post inflammatory hyperpigmentation.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Dina Abd El-nasser Attay, principal investigator, Assiut University
ClinicalTrials.gov Identifier:
NCT05099601
Other Study ID Numbers:
  • MSM
First Posted:
Oct 29, 2021
Last Update Posted:
Oct 29, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 29, 2021