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Efficacy and Safety of Using Combination of 755-nm Picosecond Alexandrite Laser and 2% Hydroquinone Compared With 2% Hydroquinone Alone for the Treatment of Melasma: a Randomized Split-face Controlled Trial

M

Mahidol University

Status

Unknown

Conditions

Melasma

Treatments

Drug: topical 2% hydroquinone
Device: 755-nm picosecond alexandrite laser with topical 2% hydroquinone

Study type

Interventional

Funder types

Other

Identifiers

NCT04597203
si 082/2019

Details and patient eligibility

About

This study aims to assess the efficacy and safety of using combination of 755-nm picosecond alexandrite laser and 2% hydroquinone compared with 2% hydroquinone alone for the treatment of melasma: A randomized split-face controlled trial

Enrollment

20 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Both male and female age 18-60 years
  • Melasma on both cheeks - epidermal or mixed type
  • Fitzpatrick Skin type III-V

Exclusion criteria

  • History of retinoid or other keratolytic drugs used within 6 months before enrolled
  • History of keloid
  • photosensitivity
  • Immunocompromised host

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups

split face - left side
Experimental group
Treatment:
Device: 755-nm picosecond alexandrite laser with topical 2% hydroquinone
split face - right side
Active Comparator group
Treatment:
Drug: topical 2% hydroquinone

Trial contacts and locations

1

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Central trial contact

woraphong Manuskiatti, M.D.; Chadakan Yan, M.D.

Data sourced from clinicaltrials.gov

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