TCTR20210311002
Recruiting
Phase 2
A Comparative study of efficacy and safety of combination treatment with oral minocycline and narrowband UV-B phototherapy versus narrowband UV-B alone in generalized vitiligo
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- generalized vitiligo
- Sponsor
- Srinakharinwirot University
- Enrollment
- 44
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subject (man or woman) is older than 18 years old
- •Subject with generalized vitiligo with a body surface area involved \>10%
- •Subject is able to recieve phototherapy treatment twice a week for 12 weeks
- •subject is willing to participate in research project with sign the inform consent before attend the study and can be responsible to treatment along total course.
Exclusion Criteria
- •subject has recieved in the 3 month prior to enrolment the following therapies; phototherapy, any immunomodulator, systemic corticosteroids and any antioxidants.
- •subject has recieved the topical treatment (topical corticosteroids, topical vitaminD) within 2 weeks of enrolment.
- •subject has a history of radiotherapy, chemotherapy or immunosuppressive therapy
- •subject has a history of skin cancer,photosensitivity or photomediatied disorders and claustrophobia
- •subject has been diagnosed as renal failure or liver disease.
- •subject has an abnormal liver enzyme test (AST,ALT) ,eGFR\<60mg/ml and ANA titer more than 1:160
- •sudject has a history of allergy to tetracyclines.
- •subject is pregnant(as determined by LMP)or subject is breastfeeding.
Outcomes
Primary Outcomes
Not specified
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