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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04740268
Other study ID # 1114
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 23, 2022
Est. completion date October 12, 2023

Study information

Verified date January 2023
Source Universal Skincare Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This pilot study will expand knowledge and application needling using the Straberi microneedling device for the improvement of Atrophic Acne Scarring


Description:

This pilot study will expand the knowledge and application of needling using the Straberi microneedling device and its safety and benefits for improving the appearance of atrophic acne scarring. The pilot aims to objectively measure skin quality using the Derma Scan, photographs, and provide objective data showing improvement by way of the Goodman and Barons quantitative scar scale.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date October 12, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 65 Years
Eligibility Inclusion Criteria: - Derma Scan showing aging including skin texture, wrinkles, brown spots, and pores. - Patients willing to sign informed consent. - Patients willing to be photographed and video documented - Patients willing to consent to 3 months of treatment Exclusion Criteria: - History of eczema in the treatment area; psoriasis and any other chronic skin conditions - History of actinic (solar) keratosis in the treatment area; - History of hemophilia - History of diabetes - The presence of raised moles, warts on the targeted area. - Collagen vascular diseases or cardiac abnormalities - Blood clotting problems - Active bacterial or fungal infection - Facial melanosis - Malignant tumors - Immunosuppression - Use of blood thinners or prednisone - Corticosteroids within two weeks of the procedure - Chronic liver disease - Porphyria or other skin diseases. - Patient not willing to sign informed consent. - TCA peels in the last 5 weeks - Subject currently has moderate to severe acne on the face. - Microneedling within the last 6 months - Subject has an active infection. - Subject has a history of a bleeding disorder - Subject has a history of keloidal tendency - Subject has received ablative or non-ablative laser treatments in the previous 6 months. - Subject has taken Accutane within the previous 3 months.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Straberi
The patient's entire face will be treated with the Straberi microneedling devise. The following settings will be used as a treatment protocol. Needle length between .02- 1.55 mm

Locations

Country Name City State
United States Lavish Beauty New York New York

Sponsors (2)

Lead Sponsor Collaborator
Universal Skincare Institute Lavish Beauty

Country where clinical trial is conducted

United States, 

References & Publications (2)

Finlay AY, Khan GK. Dermatology Life Quality Index (DLQI)--a simple practical measure for routine clinical use. Clin Exp Dermatol. 1994 May;19(3):210-6. doi: 10.1111/j.1365-2230.1994.tb01167.x. — View Citation

Goodman GJ, Baron JA. Postacne scarring: a qualitative global scarring grading system. Dermatol Surg. 2006 Dec;32(12):1458-66. doi: 10.1111/j.1524-4725.2006.32354.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Patient satisfaction of skin improvement assessed by the Goodman and Barons quantitative scar scale. A global quantitative grading system for assessing the disease load and global severity of disease in a patient with post acne scarring. The Goodman and Baron score considers type of scar, number of scars, and severity of scarring and assigns a grade 1-4 with grade 1 representing mild, macular disease and grade 4 representing severe scarring that is obviously visible at social distances of 50cm, is not easily covered by makeup, and is not able to be flattened by manual stretching of the skin. Lower scores are favorable. Scale will be completed at every office visit over the 6 month study. 6 months
Primary The Global Aesthetic Improvement Scale (GAIS) The Global Aesthetic Improvement Scale (GAIS) is a 5-point scale rating global aesthetic improvement in appearance, compared to pretreatment, as judged by the investigator 5 point scale ranging from 1 to 5 with 5 = The appearance has worsen compared with the original condition and 1 = Excellent corrective results 6 months
Secondary Overall Skin changes assessed by Derma Scan The Derma Scan System utilizes two special lighting systems (RGB +UV) and smart skin analyzer software that allows two images (before and after care) to be compared side by side, which can be used to detect the changes in skin 6 months
Secondary Overall Skin changes assessed by Acne Scar Subtypes Skin improvement assessed by Acne Scar Subtypes for improvement of acne scarring rolling, icepick, and or boxcar subtypes.Ice pick scars are narrow, sharply demarcated, V-shaped tracts, <2 mm in diameter, that extend into the deep dermis or even subcutaneous layer. Boxcar scars are wider (1-4 mm in diameter), U-shaped tracts, with sharp, vertical edges that extend 0.1-0.5 mm into the dermis. Rolling scars are characterised by dermal tethering of the dermis to the subcutis. They are generally =4 mm in diameter, irregular, with a rolling or undulating appearance.Scale will be completed at every office visit over the 6 month study. 6 months
Secondary Photographs Digital imaging device using a grid background with controlled lighting and setting to grade acne scar improvement on a quartile grading scale(1 = 1% to 25%, 2 = 26 to 50%, 3 = 51 to 75%, 4 = >76% improvement). 6 months
Secondary To evaluate the impact on the quality of life (DLQI) The Dermatology Life Quality Index questionnaire (DLQI) is 10 questions were asked to the patients and score is 0-3 for each question. The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired. 6 months
See also
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Recruiting NCT04580758 - Fractional CO2 Laser Combined With PRP Fluid Versus Gel in Treatment of Acne Scars Early Phase 1
Completed NCT01559922 - Use of Artefill® for Moderate to Severe Atrophic Acne Scar Correction Phase 3
Completed NCT02646917 - SkinPen Efficacy on Acne Scars on the Face and/or Back N/A

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