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NCT06827938Recruiting

Multicenter Real-World Study of Hyperthermia in Warts of Special Population

Multicenter Real-World Study of Hyperthermia in Skin/Mucosal HPV Infection of Special Population

Source: ClinicalTrials.gov · Last updated 14 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Hyperthermia refers to treating diseases with temperatures beyond normal body temperature (39-45℃), and moxibustion therapy of traditional Chinese medicine belongs to the category of hyperthermia. It has been reported at home and abroad that the local temperature of 44℃ can effectively mobilize the body's immunity and remove HPV infection lesions, such as condyloma acuminatum and verruca vulgaris. Our research group conducted randomized controlled experiments on patients with viral warts in the early clinical practice, and the cure rate of the hyperthermia group reached 45-55%, which was superior to the traditional method in the aspects of no trauma, low recurrence rate, easy to tolerate and so on. Our research group's preliminary research on hyperthermia of viral warts has been included in the British Medical Association's guidelines for viral warts therapy. The equipment our research group developed has been obtained the medical device registration certificate, and is in the process of national promotion. Hyperthermia is to mobilize systemic immunity through local warm heat, the preliminary clinical study of the research group shows that the therapeutic effect of hyperthermia is usually "all or none": "all" that is, after hyperthermia, all viral warts are removed, including non-treatment lesions;"None" means that some patients with viral warts do not respond to hyperthermia. Cellular immunity plays a very important role in the removal of warts. At present, some special clinical patients such as pregnant women, children, patients with autoimmune diseases, diabetes, immunosuppressants after organ transplantation and other patients with skin/mucosal HPV infection, their warts show more extensive proliferation or a longer and repeated course of disease, treatment resistance, etc. It has increased the difficulty of clinical treatment, and the specific mechanism is still unclear. Therefore, for these special populations, how to further enhance the therapeutic effect of hyperthermia is the top priority of current research. In view of the above findings, this research group intends to study the efficacy and safety of hyperthermia in the treatment of viral warts in the special population (pregnant women, children, patients with autoimmune diseases, diabetes, and immunosuppressants after organ transplantation, etc.) in a multicenter real-world study of skin/mucosal HPV infection in the special population.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
11 Feb 2025
Start date
10 Jul 2024
Primary completion date
10 Jul 2027
Lead sponsor
First Hospital of China Medical University
NCT number
NCT06827938

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From 10 Jul 2024 to the primary completion date, 10 Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • The subject suffers from tumor or other serious disease and cannot complete this clinical study

Other

  • Timely treatment and follow-up cannot be guaranteed due to personal or other objective reasons

Who the study is looking for

  • Pregnant women with viral warts
  • Diagnosis of AIDS with viral warts
  • Autoimmune disease patients with viral warts
  • Diabetic patients with viral warts
  • Patients with viral warts who are currently being treated with immunosuppressants
  • Children with viral warts
  • The subject or legal guardian is able to understand and sign the informed consent/consent to participate in the study

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
The First Affiliated Hospital of China Medical University
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ShenyangChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.