Atopic dermatitis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Group with AD patients Stored plasma samples collected from AD patients with moderate or severe pruritus in the clinical trial (jRCT2080225290) will be used. 2)Group with healthy volunteers Stored plasma samples collected from healthy volunteers who have never been diagnosed with AD in the past and are not currently diagnosed with AD in the clinical research (jRCT1030230474) will be used.
Exclusion criteria
Exclusion criteria: 1) Group with AD patients Stored plasma samples collected from AD patients with moderate or severe pruritus in the clinical trial (jRCT2080225290) will be used. 2)Group with healthy volunteers Stored plasma samples collected from healthy volunteers who have never been diagnosed with AD in the past and are not currently diagnosed with AD in the clinical research (jRCT1030230474) will be used.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This study will perform explorative analysis of the temporal variations of each metabolite, using the pre-administration measurements of healthy adults and AD patients as controls. Based on these temporal variations, we will cluster the AD patients and perform metabolites pathway enrichment analysis for each cluster. | — |
Contacts
Maruho Co.,Ltd. Kyoto R&D Center