Overview

Efficacy of Intralesional Triamcinolone Injection in the Treatment of Vitiligo

Status:
Unknown status
Trial end date:
2018-09-15
Target enrollment:
0
Participant gender:
All
Summary
A randomized split-body pilot study was planned to confirm efficacy of intralesiona triamcinolone injection in patients with vitiligo
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The Catholic University of Korea
Treatments:
Tacrolimus
Triamcinolone
Triamcinolone Acetonide
Triamcinolone diacetate
Triamcinolone hexacetonide
Criteria
Inclusion Criteria:

1. Age : 19 or older

2. A patient who voluntarily agreed to participate in the study by listening to the
explanation of the purpose and method of the study

3. A patient who has bilateral two or more vitiligo lesions with similar degree of
progression in the face or trunk

4. A patient who has no further response to excimer laser or short wavelength ultraviolet
B therapy, which is a conventional treatment for vitiligo

Exclusion Criteria:

1. Patients under the age of 19

2. Patients with enlarged or spreading lesions of vitiligo

3. Patients who do not want to do so or who refuse to write a consent form

4. Patients who are inadequate for triamcinolone acetonide administration (pregnant
women, infectious and systemic fungal infections without effective antimicrobial
agents, immunosuppression, hypersensitivity reactions to and concomitant use of
triamcinolone or its components, spontaneous thrombocytopenia, purpura, herpes
simplex, shingles, chicken pox patients)

5. Others those who are deemed unsuitable for the examination at the discretion of the
examiner