Acne Scar Clinical Trial
Official title:
A Single-Blinded Split Face Prospective Study Comparing Different Energy, Efficacy, and Safety of UltraPulse CO2 Laser in the Treatment of Acne Scar Using Antera Quantitative 3D Image Analysis
Purpose of the study is to assess the effect and evaluate topographic volume changes of UltraPulse at treating boxcar scars with different energy and the effect of UltraPulse at treating icepick scars.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | November 28, 2021 |
Est. primary completion date | September 8, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | Inclusion Criteria: - Subjects have to be aged from 20 to 60 year-old - Subjects currently have an area of involvement approximately 2cm × 2cm on each side of the face over the temples or cheek bone area - Classified as mild to moderate acne scar according to global severity of facial acne scar (GSAAS) score - After evaluation by clinician, those subjects to be treated with "Lumenis"CO2 Laser System (UltraPulse) can benefit from this laser treatment - Subjects need to be fully functional and aware of the pros and cons of the study. Subject is capable to make self judgement and sign the inform consent under his/her own will - Others: Have fully understand about this study and is willing to cooperate with the instruction of the study Exclusion Criteria: - Those who were known to have keloid formation - Those who have porphyria or known photosensitivity - Those who previously underwent laser therapy treatment or skin biopsy and have showed poor result or adverse effect - Those who were classified as "severe" according to GSAAS system - Those who have bleeding tendency - Those who present with clinical data suggesting abnormal platelet function or coagulation disorder (such as prolonged aPTT or PT) - Those that are currently taking anticoagulants or anti-platelet drugs - Those who are on aspirin or other NSAIDs - Those who have history of granulomatous or connective tissue disease - Female subjects with a positive pregnancy test - Women who refuse to stay on effective contraception or refuse pregnancy tests during the study - After evaluation by the clinician, those that have been enrolled in clinical studies over the past 6 months that may alter the current study result - After evaluation by the clinician, those currently or had previous treatment of atrophic acne scars with fillers, lasers, deep chemical peels, or any other medical or surgical treatment which in the investigators' opinion could alter the results of the current clinical study - Those that are currently taking photo-sensitive drugs, oral isotretinoin, iron supplement or other herbal medication - Those that have received laser treatment over the lesion area over the past 3 months - Those that are currently pregnant or breastfeeding - After evaluation by the clinician, and concluded underline epilepsy, area to be treated is under infection or ulceration, poor wound healing) |
Country | Name | City | State |
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Taiwan | HAUTE BEAUTÉ Skin & Vein Clinic | Taipei |
Lead Sponsor | Collaborator |
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Haute Beauté Skin & Vein Clinic | Lumenis Ltd., Taipei Medical University Shuang Ho Hospital |
Taiwan,
Alster TS, Li MKY. Microneedling of Scars: A Large Prospective Study with Long-Term Follow-Up. Plast Reconstr Surg. 2020 Feb;145(2):358-364. doi: 10.1097/PRS.0000000000006462. Erratum in: Plast Reconstr Surg. 2020 May;145(5):1341. — View Citation
Arsiwala SZ, Desai SR. Fractional Carbon Dioxide Laser: Optimizing Treatment Outcomes for Pigmented Atrophic Acne Scars in Skin of Color. J Cutan Aesthet Surg. 2019 Apr-Jun;12(2):85-94. doi: 10.4103/JCAS.JCAS_171_18. — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Topographic volume changes of acne scars from baseline one month and three month after the 2nd treatment session | Topographic volume changes of acne scars from baseline one month and three month after the 2nd treatment session | from baseline one month and three month after the 2nd treatment session | |
Primary | Histological change in epidermal/dermal component including elastic fiber and collagen synthesis three month after the 2nd treatment session from baseline | Histological change in epidermal/dermal component including elastic fiber and collagen synthesis three month after the 2nd treatment session from baseline | three month after the 2nd treatment session from baseline | |
Secondary | Access improvement of acne scar by Scale for global severity of facial acne scar from baseline one month and three month after the 2nd treatment session in both the low and high energy treated arm | Access improvement of acne scar by Scale for global severity of facial acne scar from baseline one month and three month after the 2nd treatment session in both the low and high energy treated arm. The minimum and maximum values of Scale for global severity of facial acne scar are 0 and 5, and higher scores mean a worse outcome. | from baseline one month and three month after the 2nd treatment session | |
Secondary | Compare the difference of improvement of acne scar by Scale for global severity of facial acne scar in the low versus high energy treated arm | Compare the difference of improvement of acne scar by Scale for global severity of facial acne scar in the low versus high energy treated arm. The minimum and maximum values of Scale for global severity of facial acne scar are 0 and 5, and higher scores mean a worse outcome. | from baseline and three month after the 2nd treatment session | |
Secondary | Compare the difference of newly synthesis collagen and elastic fiber through staining in the low versus high energy treated arm | Compare the difference of newly synthesis collagen and elastic fiber through staining in the low versus high energy treated arm | from baseline and three month after the 2nd treatment session | |
Secondary | Assess the frequency and severity of encountered side effects in the low versus high energy treated arm | Assess the frequency and severity of encountered side effects in the low versus high energy treated arm | from baseline and three month after the 2nd treatment session | |
Secondary | Subjects' satisfaction score rated in a 0 to 10 point scale | Subjects' satisfaction score rated in a 0 to 10 point scale | after the 2nd treatment session?one month and three month after the 2nd treatment session |
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