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New Treatment of Common Wart

Evaluation Of Intralesional Platelet-Rich Fibrin Versus Intralesional Vitamin D In Treatment Of Common Warts

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07543926
Enrollment
70
Registered
2026-04-22
Start date
2026-04-06
Completion date
2026-12-30
Last updated
2026-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Common Warts (Verruca Vulgaris)

Keywords

PRF injection

Brief summary

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.

Interventions

BIOLOGICALPRF group

intralesional PRF injection in common warts

DRUGVitamin D

intralesional vitamin D injection in common wart

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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 .

Design outcomes

Primary

MeasureTime frameDescription
treatment of common wart by PRF injection ( Mild response: < 50% reduction in lesion size , Moderate response: ≥ 50% reduction in lesion size , to measure the change in lesion size , is the patient satisfied or not )1 session every 2 weeks for 3 monthstreatment of common wart by intralesional injection of PRF
changes in common warts after treatment by PRF (measuring complete clearance and recurrence of the lesions ,asking about patient satisfaction )6 months after the last session

Countries

Egypt

Contacts

CONTACTbasma alaaeldin mohamed, resident
basmaelbolok2025@gmail.com01093827856

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 23, 2026