About this trial
This study aims to evaluate the efficacy and safety of intralesional injections of candida antigen, polidocanol sclerotherapy and combined candida antigen with polidocanol in treatment of patients with common warts.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age group: >18years.
Confirmed diagnosis by clinical and dermoscopic examination of common wart will be made.
Disqualifiers
Patients who receive any treatment for wart in the last month before the study.
Patients with history of renal or liver disease.
Patients with any evidence of bleeding diathesis, vaso-occulusive or thrombo-embolic disorders.
Pregnant and lactating females.
Trial design
Parallel
Treatments tested in this trial
polidacanol 3%
DrugAethoxysklerol 3%,60mg/ ml ampoule, kreussler pharma, Germany
candida antigen
Biological/Vaccinedelayed type of hypersensitivity reaction is induced toward the injected antigen and the wart virus as well. This can increase the ability of the immune system to recognize and eradicate the human papillomavirus on various parts of the body and eliminate the necessity of local treatment for each wart
Treatment groups
Trial outcomes
Primary outcomes
size of warts
measured by ruler) with photographic comparison at base line and before each session and one month after last session in relation to baseline lesion to detect response to therapy
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: