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Infrared Bioeffect System for the Treatment of Onychomycosis

A Multicenter Clinical Trial of Infrared Bioeffect System for the Treatment of Onychomycosis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06036654
Enrollment
60
Registered
2023-09-14
Start date
2023-02-24
Completion date
2024-08-24
Last updated
2023-09-14

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

Conditions

Hyperthermia

Keywords

hyperthermia, onychomycosis

Brief summary

Onychomycosis is a common nail plate infection caused by dermatophytes, non-dermatophytic molds, and yeasts. The disease is difficult to achieve self-healing and predisposed to secondary bacterial infections. There are currently multiple medications that can be used for the treatment of onychomycosis. The limitations are high recurrence rate and high cost, time-consuming and drug interactions. Several FDA approved laser devices have been available for the treatment of onychomycosis since 2010. As an emerging physical therapy modality, laser and light have advantages including extensive applicable range, simple operation, less trauma, and it will not lead to generation of new resistant strains. Therefore, it has been popularized and applied in clinics, especially among elderly, immunocompromised patients, or those with liver and kidney dysfunction. Laser systems in the near-infrared spectrum (780 nm∼ 3,000 nm wavelength), which are commonly used in onychomycosis, exert their effect by direct heating of target tissues, but it can cause unbearable physical pain to the patient. Compared with laser, controllable infrared bioeffect system has the advantages of high safety, less trauma, and less pain. Reported in the literature, it has been observed that regression of distant, untreated skin lesions in patients treated locally with controllable infrared bioeffect system, especially in inflammatory skin diseases such as viral warts and sporotrichosis. The aim of the research is to evaluate the safety and efficacy of controllable infrared bioeffect system in treatment of onychomycosis.

Detailed description

Mild local hyperthermia with a certain temperature range has been successfully used in treatment of some diseases. It has been applied in the treatment of some neoplasm, fungal and HPV infections. Previous studies regarding viral warts and sporotrichosis found that in patients with multiple lesions, the clearance of the target lesion is commonly followed by clearance of other distant lesions, a phenomenon suggesting that local hyperthermia could aid in establishing a specific immune response to eliminate pathogenic microorganisms. Investigators speculate that mild local hyperthermia was a potential treatment for onychomycosis. A prospective single arm clinical trial was conducted to evaluate the effectiveness and safety of mild local hyperthermia in the treatment of onychomycosis. Participants with onychomycosis with at least 2 nails involved were included. The treatment effect of the treated and the untreated nail onychomycosis was measured after 6 months and 12 months of initial treatment.

Interventions

DEVICEinfrared thermotherapy instrument

Only a single target nail was chosen among multiple onychomycosis to receive local hyperthermia treatment.

Sponsors

Jining Medical University
CollaboratorOTHER
Binzhou Medical University
CollaboratorOTHER
Gao Xinghua
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Local hyperthermia for the Treatment of Onychomycosis

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Male and female patients between 18 and 70 years old. 2. Patients with Onychomycosis confirmed by clinic and microscopic examination or culture of fungi. 3. All subjects voluntarily joined this study with informed consents. 4. The subjects have good compliance and can cooperate with investigators follow-up study.

Exclusion criteria

1. The patients during the period of pregnancy or breastfeeding. 2. The systemic and topical antifungal drugs were withdrawn 1 year and 3 months before enrollment, respectively. 3. Patients who suffered from progressive disease, autoimmune, tumor diseases or other diseases adjudged by the investigator to be inappropriate for inclusion into the study. 4. Other conditions adjudged by the investigator to be inappropriate for inclusion into the study.

Design outcomes

Primary

MeasureTime frameDescription
Cure rate of the target nail6 months, 9 months and 12 months after the first treatmentClinical and mycological cure rate of the target nail at 6 months, 9 months and12 months after the first treatment

Secondary

MeasureTime frameDescription
Cure rate of non-targeted nail6 months, 9 months, 12 months after the first treatmentClinical and mycological cure rate of non-target nail at 6 months, 9 months and12 months after the first treatment

Countries

China

Contacts

Primary ContactXinghua Gao, PhD
gaobarry@hotmail.com+86 13940152467

Outcome results

None listed

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