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Ultrasound imaging demonstration of the improvement of non-ablative laser remodeling by concomitant daily topical application of 0.05% retinaldehyde
Study Design
Subject Type
Human
Trial Design
Double-Blind, Randomised, Controlled
Trial Duration
196 days
Participants
16 (16 completed)
Efficacy
Intervention(s)
Outcome
Method
Effect
Description
Non-Ablative Laser Resurfacing + Retinal
Skin Thickness
Ultrasound
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Non-Ablative Laser Resurfacing
Skin Thickness
Ultrasound
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Study Summary
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