Trials / Completed
CompletedNCT07329907
Combination Therapy for Warts: Candida Antigen vs. Topical Keratolytic
Comparative Efficacy of Topical Salicylic Acid/Lactic Acid, Intralesional Candida Antigen, and Their Combination in the Treatment of Warts: A Randomized, Assessor-Blinded, Controlled Trial
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 126 (actual)
- Sponsor
- Benha University · Academic / Other
- Sex
- All
- Age
- 5 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
Objective: To compare the efficacy, safety, and recurrence rates of topical salicylic acid/lactic acid (SA/LA) monotherapy (Group A), intralesional Candida antigen (CA) monotherapy (Group B), and their combination (Group C) for the treatment of warts.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Salicylic Acid/Lactic Acid Topical Solution | Patients receive topical application of Salicylic Acid 40% and Lactic Acid 16% once daily for up to 6 weeks. |
| BIOLOGICAL | Candida Antigen Intralesional Injection | Patients receive intralesional injection of Candida Antigen (0.1-0.3 mL) every 2 weeks for up to 6 sessions. |
| COMBINATION_PRODUCT | Candida Antigen and Salicylic Acid/Lactic Acid | Patients receive intralesional injection of Candida Antigen (0.1-0.3 mL) every 2 weeks for up to 6 sessions, with topical Salicylic Acid 40% and Lactic Acid 16% applied in between. |
Timeline
- Start date
- 2023-12-01
- Primary completion
- 2024-06-01
- Completion
- 2024-12-30
- First posted
- 2026-01-09
- Last updated
- 2026-01-09
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07329907. Inclusion in this directory is not an endorsement.