Panelist Question: 833.530.7596

Study Number: C26-D096

Perioral Dermatitis

Study Description

This study is being done at one clinic to see how well a topical concentrate works for people with a flare-up of perioral dermatitis. Women and men will use the product for 4 weeks, and the study will evaluate improvements in the appearance of the skin and how well the product is tolerated.
Compensation: Up to 275.00

Location

Dallas Research Center: 1801 N. Glenville Dr., Suite 250 Richardson, Texas 75081

Demographic

Gender: Male or Female
Age: 18-60 years Old
Skin Type: Fitz I-VI

Requirements

Must:

  • Have a visible flare-up of perioral dermatitis.
  • Be willing to stop topical acne or perioral dermatitis treatments for at least 2 weeks before the study and throughout the study (except the study product).
  • Be willing to avoid facial treatments (Botox, fillers, lasers, chemical peels, IPL, facials, etc.) during the study.
  • Men must have little or no facial hair (or be willing to shave before study visits).
  • Be willing to attend all study visits and have study photographs taken.

 

Cannot:

  • Have allergies to skincare products or study products (azelaic acid).
  • Be using oral antibiotics or certain prescription acne/skin medications within the required washout period.
  • Have used Accutane (isotretinoin) within the past 6 months.
  • Have active skin infections or other facial skin conditions (other than perioral dermatitis) that could interfere with the study.
  • Have had facial cosmetic procedures (Botox, fillers, laser treatments, IPL, chemical peels, etc.) within the past 6 months.
  • Be taking immunosuppressive medications, systemic or topical corticosteroids, or undergoing chemotherapy/radiation.

Visit 1 Requirements:

  • Avoid application of any topical moisturizing products to the face for at least 24 hours prior to visit 1.
  • Bring a valid government-issued ID or passport.
  • If unable to attend, please contact us as soon as possible at 833-530-7596.

How to Apply

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