Mediterranean Diet vs no Dietary Intervention for Improving Signs and Symptoms of Psoriasis in Patients Treated With Anti-IL-17 or Anti-IL-23 Inhibitors - Trial NCT06399432
Access comprehensive clinical trial information for NCT06399432 through Pure Global AI's free database. This phase not specified trial is sponsored by Neil Korman and is currently Recruiting. The study focuses on Psoriasis. Target enrollment is 36 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Neil Korman
University Hospitals Cleveland Medical Center
Timeline & Enrollment
N/A
Oct 18, 2022
Jul 01, 2026
Primary Outcome
Percentage of participants who had a change in blood monocytes profiles.,Percentage of participants who had a change in T-cell profiles.,Change in blood monocyte profile.,Change in T-cell profiles.
Summary
In this study, participants will have 3 or 4 total study visits over approximately 10 total
 weeks. There is a two week medication washout period in between the 1st and 2nd visits. This
 washout only applies if participants are using a prohibited psoriasis medication (such as
 topical steroids or oral psoriasis medications, like methotrexate). During the washout
 period, participants will have to stop the prohibited medication(s). If participants are not
 using any prohibited medications, then the 1st and 2nd visits can be combined and
 participants will only have 3 total in-person visits. Participants will be randomly assigned
 (by chance; like flipping a coin) to either the Mediterranean Diet or no dietary
 intervention. After 4 weeks on the diet, participants will start treatment with either
 Anti-IL-17 or Anti-IL-23 therapy. The biologic treatments will prescribed by the participants
 regular dermatologist and not as a part of the study.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06399432
Non-Device Trial

