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Status unknownNCT03923062Updated Jan 13, 2020

Different Dermatological Approaches the Treatment of Melasma

A Phase 4 interventional study of chemicalpeeling and cryopeeling in Melasma, sponsored by Assiut University. Status unknown. Open to participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2020-01-13.

Sponsored by Assiut University · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2020), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
All
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Study summary

To compare the efficacy and safety of cryopeeling (using Liquid Nitrogen) and tranexemic acid (cyclokapron) versus chemical peeling (using TCA 20%) in treatment of melasma.

Read the detailed description

Melasma is a common, acquired, circumscribed hypermelanosis of the sun-exposed skin, It presents as symmetric, hyperpigmented macules having irregular, serrated, and geographic borders , The most common locations are the cheeks, upper lips, the chin and the forehead, but other sun-exposed areas may also be occasionally involved .

Studies has indicated the role of several risk factors such as genetics, sunlight, age, gender, hormones, pregnancy, thyroid dysfunction, cosmetics and medications .

Histologic features of melasma include an increase in the content of both epidermal and dermal melanin, but the quantity varies with the intensity of hyperpigmentation. In addition, most studies show no quantitative increase in melanocytes; however, the cells are enlarged with prominent and elongated dendrites and more abundant melanosomes. Additional features of the involved skin include solar elastosis and increased mast cells, dermal blood vessels, and expression of vascular endothelial growth factor.

Commonly used topical agents for the treatment of melasma include hydroquinone, azelaic acid, kojic acid, glycolic acid, salicylic acid and tretinoin. Of these treatments, hydroquinone remains the gold standard .Second-line treatments, such as chemical peels and lasers, are efficacious in some patients .

Chemical peeling is the application of a chemical agent to the skin, which causes the controlled destruction of a part or of the entire epidermis with or without the dermis, leading to exfoliation and removal of superficial lesions, followed by regeneration of new epidermal and dermal tissues [khunger, 2008]. The mechanism of action in melasma is the removal of unwanted melanin via controlled chemical burn of the skin .

Trichloroacetic acid has been used as a peeling agent for a long time and is still the most effective and safest agent for medium peeling, Its depth of penetration depends on the TCA concentration and on the preparation of the skin, specially the degreasing. Between 10% and 30% concentration is considered a superficial peel; above 30% provides a medium-depth peel.

Cryopeeling is a technique that uses cryotherapy in a diffuse manner throughout the skin region affected by sun damage in order to promote cell renewal and desquamation, with possible benefits in the appearance of new lesions caused by photodamage. Up to the investigator's knowledge, few studies were performed evaluating such technique.

Recently, trans-4-(Aminomethyl) cyclohexanecarboxylic acid, or tranexamic acid (TA), has been proposed as a new treatment for melasma.The main mechanism of the hypopigmentant effects of TA is due to its antiplasmin activity .In addition, TA is similar to tyrosine in a portion of its structure, which can inhibit tyrosinase competitively .Also, Plasmin transforms the vascular endothelial growth factor (VEGF) into a diffusing form, and histological examination showed that TA plays an important role in the reduction of erythema and vascularities and the number of mast cell in the dermis.Various forms of TA are used orally, topically and as a microinjection for the treatment of melasma.

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Conditions studied

  • Melasma

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03

In context

Melanosis

149 studies on the registry are indexed under Melanosis; 38 are open to participants now.

This study's planned enrollment of 40 is close to the median of 40 across 139 interventional studies indexed under Melanosis.

Browse Melanosis studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • -Subjects presented with melasma.
  • Age 20-40 years old.
  • Melasma persisting for more than 6 months that has failed to respond to conventional treatment with hydroquinone or other topical lightening agents.

Exclusion criteria

Exclusion Criteria:

  • -History of photosensitivity, keloids, hypertrophic scarring and post- inflammatory hyperpigmentation.
  • Pregnancy and lactation.
  • Subjects with local inflammatory skin disorder or active herpes infection at the site of procedure.
  • Subjects with history of medical diseases which contraindicate cryosurgery such as; cold intolerance, cold urticaria, Raynaud's disease and history of allergic reactions to cryosurgery.
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    G I A (right side): will be treated by chemical peeling

    right sideof patient's face will be treated by chemical peeling( Trichloroacetic acid 20% concentration).

    Device: chemicalpeeling

  • Experimental
    G I B(left side):will be treated by cryopeeling

    left side of the patient's face will be treated by cryopeeling using Liquid Nitrogen.

    Device: cryopeeling

  • Experimental
    G II A (right side): will be treated by chemical peeling

    right sideof patient's face will be treated by chemical peeling( Trichloroacetic acid 20% concentration).

    Device: chemicalpeeling

  • Experimental
    G II B (left side):will be treated by tranexemic acid

    left side of patient's face will be treated by tranexemic acid(cyclokapron)

    Combination Product: microneedling

Interventions

  • Devicechemicalpeeling

    Cleansing and degreasing the face with alcohol . * The patients must be sitting at an angle of 45. * A 2 × 2 cm cotton gauze will be used to apply TCA 20%. * We will apply the acid from the midline to the right side of the forehead and under the right eye, covering the right cheek and perioral area. * We then will wait for a few minutes and will observe the frost developing. * The patient will be then allowed to wash her face.

    Also known as: chemical peeling using Trichloroacetic acid 20%

  • Devicecryopeeling

    Cryopeeling will be performed by spraying the freezing substance(Liquid Nitrogen) on the face at 1-2cm distance and moving along the affected area until freezing appear.

    Also known as: cryopeeling using Liquid Nitrogen

  • Combination productmicroneedling

    Tranexamic acid will be used in aconcentration of 4mg/ml ,1ml will be used fo half of the face. * After gentle cleansing, topical analgesic cream will be applied over the area to be treated. * The microneedles will be used, the skin will be stretched and microneedling will be carried out in vertical, horizontal, and both diagonal directions for about four to five times. Tranexamic acid, 0.5 to 1 ml (4 mg/mL), will be applied over this area, and the procedure will be repeated four to five times in the above-said directions

    Also known as: microneedling using tranxemic acid

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What researchers measure

Primary outcomes

  1. melasma area and severity index (MASI)

    Clinical evaluation of melasma severity will be done by melasma area severity index (MASI) every session and at the end of treatment. No response, no improvement. * Mild response, \<25% improvement. * Moderate response, 25% to \< 50% improvement. * Good response, 50% to \< 75% improvement. * Very good response, \>75% improvement.

    Time frame: baseline

  2. photo of the patient

    photo of the patient before and after treatment

    Time frame: baseline

  3. Biopsy

    A punch biopsy will be taken from affected area for histipathological examination

    Time frame: baseline

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Kim EH, Kim YC, Lee ES, Kang HY. The vascular characteristics of melasma. J Dermatol Sci. 2007 May;46(2):111-6. doi: 10.1016/j.jdermsci.2007.01.009. Epub 2007 Mar 23. PubMed 17363223 ↗
  • Hexsel D, Rodrigues TC, Dal'Forno T, Zechmeister-Prado D, Lima MM. Melasma and pregnancy in southern Brazil. J Eur Acad Dermatol Venereol. 2009 Mar;23(3):367-8. doi: 10.1111/j.1468-3083.2008.02885.x. Epub 2008 Jul 7. No abstract available. PubMed 18631207 ↗
  • Sheth VM, Pandya AG. Melasma: a comprehensive update: part I. J Am Acad Dermatol. 2011 Oct;65(4):689-697. doi: 10.1016/j.jaad.2010.12.046. PubMed 21920241 ↗
  • Moin A, Jabery Z, Fallah N. Prevalence and awareness of melasma during pregnancy. Int J Dermatol. 2006 Mar;45(3):285-8. doi: 10.1111/j.1365-4632.2004.02470.x. PubMed 16533230 ↗
  • Sheth VM, Pandya AG. Melasma: a comprehensive update: part II. J Am Acad Dermatol. 2011 Oct;65(4):699-714. doi: 10.1016/j.jaad.2011.06.001. PubMed 21920242 ↗
  • Sarkar R, Bansal S, Garg VK. Chemical peels for melasma in dark-skinned patients. J Cutan Aesthet Surg. 2012 Oct;5(4):247-53. doi: 10.4103/0974-2077.104912. PubMed 23378706 ↗
  • Monheit GD, Chastain MA. Chemical peels. Facial Plast Surg Clin North Am. 2001 May;9(2):239-55, viii. PubMed 11457690 ↗
  • Perper M, Eber AE, Fayne R, Verne SH, Magno RJ, Cervantes J, ALharbi M, ALOmair I, Alfuraih A, Nouri K. Tranexamic Acid in the Treatment of Melasma: A Review of the Literature. Am J Clin Dermatol. 2017 Jun;18(3):373-381. doi: 10.1007/s40257-017-0263-3. PubMed 28283893 ↗
  • Na JI, Choi SY, Yang SH, Choi HR, Kang HY, Park KC. Effect of tranexamic acid on melasma: a clinical trial with histological evaluation. J Eur Acad Dermatol Venereol. 2013 Aug;27(8):1035-9. doi: 10.1111/j.1468-3083.2012.04464.x. Epub 2012 Feb 13. PubMed 22329442 ↗
  • Sharma YK, Gupta A. Some Other Serendipitous Discoveries in Dermatology. Indian J Dermatol. 2016 Jan-Feb;61(1):95-6. doi: 10.4103/0019-5154.174045. No abstract available. PubMed 26955108 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 13, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03923062
Lead sponsor
Assiut University
Responsible party
Shimaa Hafez (Principle investigator, Assiut University) — Principal investigator
First posted
Apr 22, 2019
Start date
Feb 1, 2020 (estimated)
Primary completion
Oct 1, 2020 (estimated)
Completion
Dec 1, 2020 (estimated)
Last update
Jan 13, 2020

Study contacts

Shimaa Hafez, M.B.B.CH
Contact
shimaahafez75@gmail.com
01013881659 ext. 0020
Doaa Samir, Ph.D
Contact
doaasamir1@Yahoo.com
01143387171 ext. 0020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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