allergic contact chielitis
Conditions
Interventions
Case series:patch test
Sponsors
Shanghai Skin Disease Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Male or female 18-65 years old; (2) Subjects voluntarily complete the informed consent; (3) Volunteer to participate in this study and comply with the requirements of the test, and respond to any discomfort in a timely manner; (4) The subject is clinically assessed or pathologically diagnosed with contact labitis, with or without peroral dermatitis and/or keratitis; (5) There is no serious damage to the subject's lips or test site; (6) The subject shall ensure that no skin ripping, cupping, acupuncture or other treatments are performed on the test site during the test; (7) The subject is able to accept the patch test and willing to undergo the instrument test; (8) No pregnancy or breast-feeding plan was made throughout the study period, and pregnancy was avoided during the study period; (9) Subjects who are using hormone replacement therapy or hormone birth control shall be able to ensure that they maintain their original use habits during the trial period, and subjects who are not using these hormones shall ensure that they do not use these hormones during the trial period; (10) Subjects who are taking nutritional supplements should maintain their original eating habits during the study period, and explain to the Research Center; (11) There was no oral corticosteroid therapy for nearly a month; (12) The subjects can receive the treatment plan and make regular follow-up visits as required by the project.
Exclusion criteria
Exclusion criteria: (1) Lactating or pregnant women; (2) Subjects frequently or recently used medications that may interfere with the trial (e.g., oral steroids, anti-inflammatory drugs, montelukast, inhaled for more than 3 months or insulin); (3) Subjects with chronic diseases (such as insulin-dependent diabetes mellitus, lupus, rheumatoid arthritis, or other immune/autoimmune diseases) that may affect the study; (4) the subject has a tumor, has been or is currently receiving treatment for tumor, or is currently taking any cancer prevention medication; (5) Those who are exposed to the sun regularly or outdoor workers; (6) Having a cold, fever or other serious illness during the test; (7) Have had facial surgery or cosmetic treatment within 6 months; (8) A history of hyaluronic acid, botox and other injections in the test site within 4 weeks; (9) Other clinical or cosmetic tests shall be conducted in the test area 7 days prior to the start of the test; (10) Highly sensitive to physical conditions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| positive rate; | — |
Countries
China
Contacts
Public ContactYiyi Zhang
Shanghai Skin Disease Hospital
Outcome results
None listed