Status:

RECRUITING

Development of Products Based on Secretom From Stem Cell Conditioned Medium for Melasma Therapy

Lead Sponsor:

Dr.dr.Irma Bernadette, SpKK (K)

Conditions:

Melasma

Eligibility:

FEMALE

30-60 years

Phase:

NA

Brief Summary

This research is a clinical study with a single-blind randomized clinical trial design (randomized controlled trial) in RSCM-FKUI This study aims to Assess the effectiveness and safety of intradermal...

Detailed Description

Melasma is a pigmentation disorder in the form of brownish macules with irregular edges caused by dysfunction of melanogenesis. Melasma occurs more often in women with Fitzpatrick skin types IV-VI, na...

Eligibility Criteria

Inclusion

  • Women diagnosed with melasma.
  • Women without melasma and have areas of skin that are clinically free of lesions for SP control.
  • 30-60 years old.
  • Fitzpatrick skin type IV-V.
  • Willing to be a research subject by signing a research consent form (Informed Consent).

Exclusion

  • Pregnant and breastfeeding women.
  • Currently using hormonal contraception or have ever used contraception hormones in the last 6 months.
  • Using topical therapy for melasma, for example corticosteroids, tretinoin, hydroquinone, and other therapies that whiten or brighten the skin in the last 2 weeks.
  • Using topical triple combination cream therapy for at least 3 months and did not show significant improvement
  • Using systemic therapy for melasma, for example antioxidants or tranexamic acid in the last 4 weeks.
  • History of superficial peeling therapy in the last 4 weeks.
  • History of deep peeling therapy, laser or mechanical abrasion in the last 6 months.
  • Using drugs that are photosensitizers such as tetracycline, phenytoin, carbamazepine, spironolactone.
  • History of blood clotting disorders or on blood thinning therapy.
  • Allergy to tranexamic acid.
  • Have other skin complaints that may interfere with the evaluation of melasma, for example post-inflammatory hyperpigmentation, Hori's nevus, Ota's nevus, pigmented contact dermatitis, and other pigmentation disorders
  • Difficulty complying with treatment.

Key Trial Info

Start Date :

February 13 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 30 2025

Estimated Enrollment :

90 Patients enrolled

Trial Details

Trial ID

NCT06516419

Start Date

February 13 2024

End Date

March 30 2025

Last Update

July 24 2024

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Clinical Research Supporting Unit- Faculty of Medicine, University of Indonesia

Jakarta Pusat, DKI Jakarta, Indonesia, 10430

2

Dr. Cipto Mangunkusumo Hospital

Jakarta Pusat, DKI Jakarta, Indonesia, 10430