Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:18 AM
Ignite Modification Date:
2025-12-25 @ 2:18 AM
NCT ID:
NCT01098734
Eligibility Criteria:
Inclusion Criteria:
* Clinical diagnosis of chronic atopic dermatitis (Hanifin's criteria) for greater than 6 months with a minimum of 5% and a maximum of 20% BSA.
* IGA scores of 2-4 at Day 0.
* WOCBP must have a negative serum beta-hCG pregnancy test before randomization, and they and their male partners must take pregnancy precautions for the duration of the study, as also must male patients.
* Willing to comply with Protocol and attend all visits.
* Provide written informed consent prior to entering study procedures.
* Patient has no latent or active tuberculosis infection according to medical history or current examination and tests.
Exclusion Criteria:
* Pregnancy or lactation.
* Spontaneously improving or rapidly deteriorating atopic dermatitis.
* Presence of atopic dermatitis on only hands and/or feet.
* Any skin disease other than atopic dermatitis that might interfere with clinical assessment or put patient at risk.
* Active allergic contact dermatitis or other non-atopic forms of atopic dermatitis.
* Other concommitant serious illness or medical condition, virus or renal insufficiency, or clinically significant abnormality that could put patient at risk during the study.
* History of neurological/psychiatric disorders including psychotic disorders, dementia or any other reason that would interfere with the patient's participation.
* Systemic immunomodulatory therapies for other conditions within 4 weeks prior to the baseline visit.
* Any phototherapy, photochemotherapy or systemic atopic dermatitis therapy within 2 weeks of the baseline visit.
* Prolonged exposure to natural or artificial sources of UV within 4 weeks prior to baseline visit or intention to have such exposure during the study.
* Topical atopic dermatitis therapies (including corticosteroids and calcineurins) in the areas to be treated within 2 weeks prior to baseline.
* Alcohol abuse in the last 2 years.
* Allergic history to any of the non-medical ingredients of the study cream.
* Treatment with an investigational drug within one month of Day 0 or current participation in another clinical trial.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01098734
Study Brief:
Protocol Section:
NCT01098734