Straberi Microneedling For Atrophic Acne (SAA)

Universal Skincare Institute

Status: Completed

Conditions: Atrophic Acne Scar

Treatments: Device: Straberi

Study type: Interventional

Funder types: Other

Identifiers

NCT04740268

1114

Details and patient eligibility

About

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

Full 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.

Enrollment: 25 patients

Sex: All

Ages: 21 to 65 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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25 participants in 2 patient groups

Patiant without treatment

Other group

Description:

Non-Randomized patients with atrophic acne skin conditions

Treatment:

Device: Straberi

Straberi Microneedling Treatment

Other group

Description:

Non-Randomized treatment for patients with atrophic acne skin conditions using the Straberi Microneedling device.

Treatment:

Device: Straberi