

Improving the health of our patients through groundbreaking clinical research
The Schweiger Dermatology Group (SDG) Clinical Research Department Research Clinic is led by Dr. David Goldberg, founder of Skin, Laser and Surgery Specialist of New York and New Jersey. Dr. Goldberg brings more than 25 years of experience in conducting large multi-center clinical trials on a wide variety of cosmetic and medical devices, as well as pharmaceutical treatments. Our research team is committed to responsible research conducted under strict industry and safety standards.
Purpose: To evaluate the safety and efficacy of the investigational Cutera® 1726 nm laser system (also referred to as ‘Alice’) for the treatment of mild to severe acne vulgaris. Subjects will receive three 1726 nm laser treatments at 3 week intervals. Follow-up visits will occur at approximately 10 days post each treatment (via phone) and at 4-, 12-, 26- and 52-weeks post-final treatment.
Qualifications:
Duration: Approx. 18 months
Location: Hackensack, NJ
Compensation: $325
To participate contact Diana Aranzazu, [email protected], 201-951-0701
Purpose: Vitiligo is a skin condition in which there is a loss of color (referred to as “depigmentation”) from areas of skin. This results in uneven white patches that have no pigment, but the skin feels like normal. The purpose of the study you are being asked to participate in is to evaluate the safety and effectiveness of the RECELL® Device when used for repigmentation of stable vitiligo. Stable vitiligo means that the areas affected by loss of pigment have been unchanged for at least the last 12 months. The study will evaluate the effect of using RECELL for repigmentation.
Qualifications:
Duration: Approx. 52 weeks
Location: Hackensack, NJ
Compensation: If all visits kept, up to $1350 will be paid to patient *once all visits are completed*
To participate contact Diana Aranzazu, [email protected], 201-951-0701
Purpose: This research study will look at two different doses of CTP-543 compared to placebo (looks like the study drug, but does not contain active ingredients) when given to research subjects with alopecia areata (sudden hair loss) twice-daily for 24 weeks. The main purpose is to determine if CTP-543 will result in hair regrowth, and to see if taking CTP-543 is safe.
Qualifications:
Duration: Approx. 28 weeks
Location: Hackensack, NJ
Compensation: If all visits kept, up to $500 will be paid to patient *once all visits are completed*
To participate contact Diana Aranzazu, [email protected], 201-951-0701
Purpose: A clinical research study to test the effectiveness of an investigational medication to reduce symptoms.
Qualifications:
Duration: 60 weeks/visiting doctor’s office at least 16 times
Location: Hackensack, NJ
Compensation: If all visits are kept, up to $1000 will be paid to the patient *once all visits are completed*
To participate contact Diana Aranzazu, [email protected], 201-951-0701
Purpose: Simultaneous Application of High-Intensity Focused Electromagnetic Procedure and Radiofrequency for Toning of Buttocks. Subjects of both groups will be required to complete four (4) treatment visits and two follow-up visits. All of the study subjects will receive the treatment with the subject device.
Qualifications:
Duration: Approx. 12 weeks
Compensation: TBD
Purpose: To Evaluate the Effects of RENUVA® HD Treatment on Human Skin Quality and Nasolabial Fold Volume Restoration. Subject with moderate deep wrinkles to very deep wrinkles of the nasolabial folds will receive 1 treatment using Renuva on the right and left side of the face and the right infra auricular area (behind/below their ear). Subject will undergo 5 biopsy procedures of the right treated infra auricular area: pre-treatment, day 30, day 60, day 90, and day 180 after treatment to evaluate if Renuva induces Collagen and Elastin production.
Qualifications:
Duration: Approx. 6 months
Compensation: $375
Purpose: To evaluate the safety and efficacy of Sofwave treatment to lift lax tissue in the submental and neck zones and to lift the eyebrow. This study is a two-arm study. Eligible patients will receive 2-4 face and/or neck and/or submental or “off the face” (abdomen, or arms, or thighs, or Décolleté) treatments (per PI discretion, 2-12 weeks apart) using the Sofwave System. Follow up visits will be conducted at 3 and 6 months post final treatment.
Qualifications:
Duration: Approx. 6-8 months
Compensation: $240 for study visits/ $1200 for biopsies taken
Interested in participating in our clinical research study?
Contact: Diana Aranzazu
[email protected]
201-951-0701
To learn more contact: Diana Aranzazu, [email protected], 201-951-0701
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