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Not yet recruiting Not applicable NCT07543926

New Treatment of Common Wart

No applicable phase (e.g. observational)
Conditions: Common Warts (Verruca Vulgaris)

Sponsor: Sohag University

trial.available_in: БГ
Overview
this study aims to compare the efficacy and safety of platelet rich fibrin injection versus intralesional vitamin D injection in the treatmentof common warts. PRF, as an autologous biological material , may enhance tissue regeneration and immune response.
Who can participate
Inclusion Criteria: * \- Age more than or equal to 18 years * Clinically and dermoscopically confirmed Common warts of both sex * patient not receiving previous treatment at least one month before recruitment in our study * Single or multiple lesions suitable for injection. Exclusion Criteria: * Chronic Systemic desise (DM , HTN , Autoimmune , immunosuppressive disorders eg , lupus , renal or hepatic failure ) or Hematologic Conditions (anemia : hemoglobin level below 10 g/dl , thrombocytopenia : platelet count below 150,000 /µL ) Infectious Diseases , Local bacterial or fungal infection at the lesions . Pregnancy, Lactation , patients who has hypersensitivity of vitamin D .
Interventions
PRF group
BIOLOGICAL
Vitamin D
DRUG
Locations 1
Egypt (1)
Sohag University
Sohag
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
06.04.2026
Completion date
30.12.2026
Registry ID
NCT07543926
Source
clinicaltrials.gov
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