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Clinical study of simulated human radiation hyperthermia patch in the treatment of refractory viral warts

Clinical study of simulated human radiation hyperthermia patch in the treatment of refractory viral warts

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037609
Enrollment
Unknown
Registered
2020-08-29
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

Refractory viral warts

Interventions

Patients with refractory viral warts:Graphene-simulated human far-infrared radiation patch therapy

Sponsors

Xiang'an Hospital Affiliated to Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria of viral warts; 2. The patients who have no effect or relapse after routine treatment such as cryotherapy and topical medicine; 3. Patients aged 6-65 years, both male and female; 4. Patients who signed informed consent (under 14 years old, informed consent should be signed by guardian).

Exclusion criteria

Exclusion criteria: 1. In patients with local skin lesions complicated with infection, severe exudation and other skin diseases affecting the experimental results were found; 2. Patients with severe liver and kidney dysfunction, low immune function and mental disorders; 3. Patients who received systemic or topical corticosteroids or immunosuppressants 2 weeks before treatment; 4. Pregnant women and lactation patients; 5. Patients with severe liver and kidney diseases, autoimmune diseases (such as systemic lupus erythematosus, rheumatoid disease, etc.), HIV infection and malignant tumor; 6. Patients who have been allergic to this product and its related components in the past; 7. Patients who are unable to use in accordance with the requirements of clinical trials and comply with the provisions of drug restriction; 8. Patients unable to complete the treatment plan and follow-up observation; 9. Patients who do not meet the requirements of this study or are unable to participate in the study due to other reasons are judged by the researcher.

Design outcomes

Primary

MeasureTime frame
overall rate;

Secondary

MeasureTime frame
Satisfaction rate of patients;Degree of discomfort relief;

Countries

China

Contacts

Public ContactShan Shijun

Xiang'an Hospital Affiliated to Xiamen University

15822183620@163.com+86 15822183620

Outcome results

None listed

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