Cicatrix Clinical Trial
A prospective study to evaluate the efficacy and safety of FMRT for treating non-hypertrophic post-burn scars in an Asian population.
Background: Laser therapy is an emerging, minimally invasive treatment for scars. Among the
various techniques, fractional microplasma radiofrequency technology (FMRT) has proved to be
effective for various types of scars and skin conditions such as rhytids, striae distensae,
and hyperpigmentation.
Method: A prospective clinical trial was conducted to evaluate the efficacy and safety of
FMRT for treating non-hypertrophic post-burn scars in an Asian population. All patients
underwent three to five treatment sessions at intervals of 8−16 weeks. The patient and
observer scar assessment scales (POSAS) were use to evaluate changes in the burn scars
before and after treatment. Intermediate and long-term adverse events were recorded for
outcome analysis.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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