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INCYTE ECZEMA with Sleep Distrubance

This clinical trial is for adults over the age of 18 who have mild to moderate eczema (Atopic Dermatitis) with ITCH that interrupts sleep.  This is a topical product (applied to the skin directly) (Ruxolitinib cream 1.5%).  This is a Phase IV (4), Open-Label (no placebo arm) clinical trial to evaluate the reduction in sleep disturbance after using Ruxolitinib cream.  The basic criteria are listed below.  Click to sign up or request more info.

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incyte Eczema / Sleep Disturbacne (902)

Participation Information

Volunteers needed for an 8 week long treatment period (with participation lasting up to 18 weeks total).  This clinical trial is for a topical cream that is FDA approved for Atopic Dermatitis called Ruxolitinib cream 1.5%.  Stipend available up to $375.00  (5 x $75 / visit) to those who qualify and participate. 


To Qualify, you must meet the following INCLUSION CRITERIA:

1.)  18 years of age or older

2.)  Have between 3 and 20% body surface area with eczema (atopic dermatitis)

3.)  Sleep interruption due to itch from eczema (atopic dermatitis)


To Qualify, you must NOT meet the following EXCLUSION CRITERIA:

1.)  Works nighttime shifts 

2.)  Itch due to chronic liver or kidney disease

3.)  Hepatitis B or C infection (current or previous)


ClinicalTrials.gov Identifier:  NCT05696392 

https://clinicaltrials.gov/ct2/show/NCT05696392?term=ruxolitinib&cond=atopic+dermatitis&draw=2&rank=6


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