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Clinical Trial Summary

To investigate the efficacy of Erbium:Yttrium aluminum garnet laser (Er:YAG) in the treatment of enlarged pores.


Clinical Trial Description

- Enlarged pores are caused by multifactorial factors such as sex, genetics, aging, etc.

- The gold of the treatment is to recollagenesis of the dermis and resurfacing of the epidermis.

- Modalities that have been proved on their efficacy for enlarged pores treatment included topical retinoic acid, chemical peeling, intense pulsed light, radiofrequency device, laser such as Q-switched and Long Pulsed Neodymium-Doped Yttrium-Aluminum-Garnet (Nd:YAG) 1,064nm, Long pulse duration pulsed dye laser 595nm, etc.

- Er:YAG laser is an ablative laser which creates both recollagenesis and resurfacing. It ha been proved to be safe and effective in the treatment of atrophic acne scar.

- However, the efficacy of this laser for enlarged treatment has not yet been established. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02544958
Study type Interventional
Source Mahidol University
Contact
Status Active, not recruiting
Phase N/A
Start date May 2015
Completion date August 2016

See also
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Active, not recruiting NCT05784363 - A Study of NT 201 in the Treatment of Enlarged Pores and Excessive Sebum Production in the Face Phase 1
Recruiting NCT04471948 - The Safety and Efficacy of 1064-nm Picosecond Laser With Microlens Array for Pore Tightening; a Pilot Study N/A
Recruiting NCT05987319 - Feasibility Study to Collect and Assess Safety Data for a Radiofrequency Microneedling Device for Electrocoagulation and Hemostasis of Soft Tissues for Dermatologic Conditions N/A
Active, not recruiting NCT06293755 - Microneedle Patch With Botulinum Toxin in Management of Enlarged Facial Pores Phase 3