Eczema
Conditions
Interventions
Intervention group:Under the routine clinical treatment and based on the medication prescribed by the doctors from the Dermatology Hospital of Southern Medical University for treating eczema, the test
Control group:Under the routine clinical treatment and with the medication prescribed by the doctors from the Dermatology Hospital of Southern Medical University for treating eczema, no other moisturi
Sponsors
Dematology Hospital of Southern Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. 18-60 years old, healthy female or male. 2. Clinically diagnosed with mild to moderate eczema. 3. Have good compliance with this project. 4. Have good communication skills. 5. Willing to undergo follow-up and perform relevant non-invasive tests. 6. Can understand the trial process, voluntarily participate in the trial and sign a written informed consent form.
Exclusion criteria
Exclusion criteria: 1. Pregnant or lactating women, or those planning to conceive in the near future; 2. Those who have participated in other projects in the past 2 months; 3. Those who have taken oral or topical corticosteroids or other anti-inflammatory medications in the past month; 4 . Those who have received biologic therapy for eczema in the past year; 5. Those who have undergone other oral drug treatments for eczema in past month; 6. Those who are unavoidably exposed to sunlight for a long time; 7. Those with other medical conditions that may affect the trial resultssuch as a history of coagulation disorders, severe hyperglycemia, hypertension, hyperlipidemia, mental illness, or other major diseases); 8 Those who are deemed unsuitable for the trial by other clinical assessments; 9. Non-voluntary participants or those who cannot complete the specified trial content as required;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Antera 3D Image Acquisition (3D Red Zone Analysis); | — |
Secondary
| Measure | Time frame |
|---|---|
| Digital Camera Photography (of Skin Lesion Changes);Transdermal moisture loss measurement;Measurement of moisture content in the stratum corneum;Clinician Assessment (EASI Assessment);Adverse events / Serious adverse events; | — |
Countries
China
Contacts
Public ContactYe Li
Dematology Hospital of Southern Medical University
Outcome results
None listed