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Efficacy of 0.05%topical everolimus in the treatment of adenoma sebaceum in tuberous sclerosis

Phase 2
Recruiting
Conditions
adenoma sebaceum
Registration Number
TCTR20180820002
Lead Sponsor
Dermatology division, Department of internal medicine, King Chulalongkorn Memorial Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
15
Inclusion Criteria

-patients with adenoma sebaceum

Exclusion Criteria

-pregnancy
-allergic reaction to everolimus

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
improvement of adenoma sebaceum 0,4,8,12,24 weeks Photograph
Secondary Outcome Measures
NameTimeMethod
safety of 0.05% topical everolimus 0,12 weeks blood test for complete blood count ,renal function test
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