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Salicylic Acid Versus Cryotherapy for the Treatment of HPV1-induced Plantar Warts

Salicylic Acid Versus Cryotherapy for the Treatment of HPV1-induced Plantar Warts: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05617950
Enrollment
174
Registered
2022-11-16
Start date
2022-11-30
Completion date
2022-11-30
Last updated
2022-11-16

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

Conditions

Warts

Brief summary

To evaluate whether salicylic acid was superior to cryotherapy for plantar warts

Detailed description

Patients with plantar warts were randomized equally to receive salicylic acid or cryotherapy. Cryotherapy is delivered by a technician up to a maximum of four treatments 3 weeks apart. Thirty percent of salicylic acid is applied once daily by the patient (or parent) for a maximum of 12 weeks. The primary outcomes were the cure rates at 12 weeks; secondary outcomes included time to clearance of warts, patient satisfaction with the treatment and treatment-related adverse effects.

Interventions

Salicylic acid is applied once daily by the patients (or parents) for a maximum of 12 weeks.

OTHERcryotherapy

Cryotherapy is delivered by a technician up to a maximum of four treatments 3 weeks apart.

Sponsors

The 306 Hospital of People's Liberation Army
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Patients with HPV1-induced plantar warts. * Total number of warts is ≤5. * Aged 12 years or older.

Exclusion criteria

* Patients are currently participating in another trial for the treatment of plantar warts. * Patients had received two or more consecutive sessions of cryotherapy, with an interval of no more than 4 weeks (The history of salicylic acid treatment was not considered as criteria for exclusion because high concentration salicylic acid is not commercially available in Chinese mainland). * Patients have taken immunosuppressant drugs (such as oral corticosteroids) during the past three months. * Patients have impaired healing eg due to diabetes, vitamin A deficiency, hyperthyroidism and hypothyroidism. * Patients have autoimmune diseases (such as systemic lupus erythematosus, dermatomyositis, scleroderma or other diseases). * Patients are pregnant or ready for pregnancies or breast-feeding. * Patients have cold intolerance (such as cold urticaria, cryoglobulinaemia, cold agglutinin syndrome or Raynaud's syndrome). * Patients have local pain intolerance. * Patients have local hypoesthesia. * Patients are unable to tolerate salicylic acid or cryotherapy.

Design outcomes

Primary

MeasureTime frameDescription
cure rate at 12 weeks12 weeks since the initial treatmentA patient was considered to be cured if all warts were no longer visible and could not be palpated anymore.

Secondary

MeasureTime frameDescription
time to clearance of warts12 weeks since the initial treatmentThe time from treatment initiation until clearance of all warts
patient satisfaction with the treatment12 weeks since the initial treatmentPatient satisfaction was rated on a 5-point scale (from very happy to very unhappy)
treatment-related adverse events12 weeks since the initial treatmentSome adverse effects, including pain, swelling, blisters, hemorrhagic bullae, bruising, and skin breakdown, were recorded by the patients, whereas others, including secondary bacterial infection, hyperpigmentation, hypopigmentation, and scarring were evaluated by a dermatologist

Contacts

Primary ContactShichao Lu, MD
lvshichao@sina.com8610-010-66356984

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026