Psoriasis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are between 18 and 70 years old
- You can read and write in English
- You are willing to give your consent and understand what the study involves, including any possible risks
- You have been diagnosed with rheumatoid arthritis, psoriatic arthritis, psoriasis, or ankylosing spondylitis, and are currently using or have been recommended a biologic or DMARD medication to treat it
Who may not be able to join:
- You are pregnant, breastfeeding, or planning to become pregnant within the next 12 months
- You have serious liver or kidney disease
- You have previously had an organ transplant or are waiting for one
- You are currently receiving treatment for cancer
- You have a mental illness that is not well controlled, such as schizophrenia, bipolar disorder, or an active eating disorder
- You have a terminal illness
- You are currently using opioid medications
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Myles Spar, MD, AndHealth
Phone: 614-697-3296
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
PROMIS - Global Health; Routine Assessment of Patient Index Data 3 (RAPID 3); Dermatology Life Quality Index (DLQI); Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.