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MI Skin Center is expanding our clinical research program, giving patients the chance to participate in trials for various skin conditions.

Clinical trials play a vital role in advancing dermatologic care and may provide access to investigational treatments under supervision of Dr. Francisca Kartono.

Hands with red, scaley, eczema patches around the nail bed. Treatments available at MI Skin Center in Northville MI.
Arm bent showing chronic hives. Treatments at MI Skin Center in Northville MI.
A patient who is a man looking at a tablet held by a medical professional going over treatment options
A scalp with spots of hair loss. Treatments available at MI Skin Center in Northville MI.

We are seeking volunteers for clinical research studies for the following skin conditions:

Atopic Dermatitis (Eczema) – Moderate to severe cases. If advanced treatments like biologics or JAK inhibitors are being considered, clinical trials may be an option.

Hidradenitis Suppurativa (HS) – Chronic inflammatory condition affecting areas such as the underarms and groin.

Alopecia Areata – For patients who have not received prior treatment.

Pediatric Vitiligo – Clinical studies for children with vitiligo.

Chronic Spontaneous Urticaria (Chronic Hives) – Persistent hives lasting longer than 6 weeks.

Lichen Sclerosis – Chronic inflammatory skin condition affecting delicate skin areas.

How to Participate

Participants are compensated up to $5,200, and all study-related visits, testing, and study medications are provided at no cost. This is a unique opportunity to meet with Dr. Kartono and our research team while contributing to the future of dermatologic care.

Participation is voluntary, and your safety and care remain our top priority.

Call (248) 232-2629 Today

Interested in participating in a clinical trial?

By completing this form, you can request more information about available studies, eligibility requirements, and how to get involved. We're here to provide you with the details you need to make an informed decision about participation.

 FAQs

  • The goal is to improve care for people with your condition. The treatment may help your symptoms, but there are no guarantees. However, you’ll receive high-quality medical care and contribute to medical research.

  • Participation in the trial is at no cost to the patient, with no insurance involvement and no billing. You will be compensated for each visit, including reimbursement for transportation arrangements, for all trials.

  • Your privacy is a priority. Only authorized researchers and healthcare professionals will access your data, which is securely stored and usually de-identified to protect your identity.

  • Some studies require more time and effort than others. We will give you a clear schedule so you can decide if the trial fits your routine.

  • Every clinical trial follows strict safety guidelines, and participants are closely monitored. We will provide you with all known risks and side effects before you decide to join.

  • Each trial has specific criteria based on age, medical history, and previous treatments. If you don’t qualify, we may suggest other studies or treatment options.

  • Your health and safety are our top priorities. If you experience any serious side effects, doctors will take immediate action, and you can leave the study at any time.

  • Each trial is different, but participation may involve taking medication, attending check-ups, and answering health-related questions. We will provide a clear schedule outlining the number of visits and study duration.

  • Some trials allow ongoing treatments, while others have restrictions. You can continue seeing your doctor, and we will coordinate with them to ensure your care is managed properly.