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Evaluation of the Application of Intradermal Injection Therapy with Polyinosinic-polycytidylic Acid in the Treatment of Viral Warts

Evaluation of the Application of Intradermal Injection Therapy with Polyinosinic-polycytidylic Acid in the Treatment of Viral Warts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100141
Enrollment
Unknown
Registered
2025-04-03
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Viral warts

Interventions

Experimental group:Treated by intratumoral injection of podofilox
Control group:Treated by electrocautery

Sponsors

Chinese People's Liberation Army Navy Characteristic Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The clinical symptoms and signs of the patients are in line with the diagnostic criteria for viral warts in "Clinical Dermatology"; 2.The patients are aged over 14 years and under 60 years; 3.The patients have not received any pesticide treatment for viral warts before the trial; they have no severe allergy to the drugs used and are willing to adhere to the medication as prescribed by the doctor; 4.The patients have given informed consent and voluntarily participate in this clinical study.

Exclusion criteria

Exclusion criteria: 1.Patients who have been treated for viral warts; 2.Patients with any other coexisting skin diseases that may interfere with the treatment effect; 3.Patients with any history of allergy to the study drug, pregnant or lactating women, or women planning to conceive in the near future; 4.Patients with a history of systemic lupus erythematosus, rheumatoid arthritis or other immune diseases or serious systemic diseases (clear history of central nervous system, cardiovascular system, renal system, liver system, respiratory system, metabolic and musculoskeletal system), or patients currently undergoing tumor treatment; 5.Patients with abnormal renal and liver function or known chronic infectious diseases; 6.Patients with poor compliance, or those who are critically ill and unable to complete the treatment course, or those judged by the researcher to have other factors that make them unsuitable for participation in the trial.

Design outcomes

Primary

MeasureTime frame
The number of skin lesions;Size of the lesion;

Countries

China

Contacts

Public ContactWa Bo

Chinese People's Liberation Army Navy Characteristic Medical Center

m18817365409@163.com+86 188 1736 5409

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026