NCT03068156CompletedNot Applicable
Efficacy of 308-nm Excimer Laser for Primary Localized Cutaneous Amyloidosis Treatment in Asians: Pilot Study
Chulalongkorn University1 site in 1 country15 target enrollmentStarted: January 31, 2022Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Chulalongkorn University
- Enrollment
- 15
- Locations
- 1
- Primary Endpoint
- Roughness evaluation by using Visioscan® VC98
Study Overview
Brief Summary
Efficacy of 308-nm excimer laser for primary localized cutaneous amyloidosis treatment in Asians, pilot study.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Patients, aged >18 years old with lichen amyloidosis diagnosed by using clinical presentation and pathologic features
Exclusion Criteria
- •Those with cutaneous amyloidosis associated systemic diseases
- •Pregnancy or lactating woman
- •Those who are allergic to urea, olive oil
- •Those who are photosensitive to ultraviolet radiation
- •Those who had been previously treated with medications/ radiation/ laser within 3 months for systemic and 1 month for topical therapy
Arms & Interventions
excimer laser
Experimental
Intervention: 308-nm excimer laser (Radiation)
Control
No Intervention
Outcomes
Primary Outcomes
Roughness evaluation by using Visioscan® VC98
Time Frame: Change from baseline roughness at every 2 weeks up to 16 weeks
The improvement of roughness evaluation
Secondary Outcomes
No secondary outcomes reported
Investigators
Einapak Boontaveeyuwat, MD
Asst. Prof.
Chulalongkorn University
Study Sites (1)
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