A Study to Evaluate the Performance of Adex Gel in the Treatment of Atopic Eczema Using SCORAD and Quality of Life Assessments.

Patients will be recruited by the General Practitioner (GP) surgeries using their databases to identify patients who are currently atopic eczema sufferers and are using mainly emollients (other than Adex Gel) to manage their condition. Patients or their parents/guardians will be contacted by the surgery to see if they would like to participate in this study and to establish whether they are currently or have been using oral or topical corticosteroids or other immunomodulators in the previous 1 month. Advertisements in the surgery may also be used as these may encourage new eczema sufferers to ask the doctor if they could participate in this study. As new eczema patients they would not currently be using steroids for their condition so would be deemed eligible for screening.

Patients and their parents/legal guardians will attend the screening and enrolment visit where parents/legal guardians will be asked to sign an informed consent form, and where appropriate the participant will sign an assent form, confirming their agreement to take part in the study. A number of questions will be asked about medical history and current medications as well as eligibility criteria. No washout period will be implemented.

Those who are considered eligible to participate in accordance with the inclusion and exclusion criteria given in section 4.6, will then undergo their baseline assessments where the Investigator/ research nurse will perform the SCORAD assessments and record these in the patient's paper Case Report Form (CRF). The patient or their parent/ guardian will also complete a baseline quality of life questionnaire (CDLQI) and photographs will also be taken.

The patients will then be given sufficient supplies of Adex Gel (depending on the coverage of their eczema) to use over the 4 week use period (additional packs may be provided at visit 2, if necessary). They will be asked to use Adex Gel instead of their usual emollient (if already using one) and to try and refrain from using oral or topical corticosteroids, or immunomodulators for the duration of the study. If, in the opinion of the investigator, it becomes necessary for patients to use oral or topical corticosteroids or immunomodulators during the study, the Investigator/ research nurse will record this on their CRF, and the patient will be withdrawn from the study. Patients will be asked to record use of any other medication or topical products during the study in their Patient Diary.

After 2 weeks of treatment, patients will return to the GP surgery and will be asked about their compliance with the study requirements, changes in health and medications and any incidents will be recorded. They will again have their eczema assessed by the Investigator/ research nurse and the results recorded on the CRF.