High Intensity Focused Ultrasound (HIFU) Treatment of Basal Cell Carcinoma (HIFU-BCC)

Jacek Calik

Status: Enrolling

Conditions: Basal Cell Carcinoma

Treatments: Device: TOOsonix System ONE-M

Study type: Interventional

Funder types: Other

Identifiers

NCT05698706

HIFU-BCC-2023-1

Details and patient eligibility

About

The overall objective of the study is to evaluate the safety and efficacy of treatment of Basal Cell Carcinoma (BCC) using a new modality based on high-intensity focused ultrasound (HIFU). BCC is the most common type of skin cancer in Europe, Australia and the US. It accounts for more than 75% of all skin cancer cases in those regions. There are currently more the 14000 BCC cases registrations in Poland every year, and occurrences on a global scale are counted in several millions per year. Given the trend of aging population those numbers will only increase with time. Finding new and more effective treatment methods are therefore highly relevant from both a clinical and socioeconomic perspective. The investigational device used in the study is a system capable of making controlled and targeted thermo-mechanical treatment of small intradermal volumes containing e.g. BCC cells, but without inflicting damage to the surrounding tissue.

The investigation involves an evaluation of the safety and efficacy profile 3 months after a single few-minute treatment. Subsequent follow-up of secondary endpoints is done every third month until the end of the study one year after the treatment.

Enrollment: 27 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects of each gender aged 18 years or older at the time of informed consent. There is no upper limit of age.
• Subjects who have received oral and written study information, accepted participation and signed the informed consent document.
• Subjects who are willing and mentally and physically capable to understand and follow the treatment and follow-up schedule including post-treatment care instructions.
• Subjects who are willing to have photographs and images taken of the treated lesions to be used anonymously or coded in evaluations and publications.
• Subjects, who have histologically and clinically verified basal cell carcinoma cancer of thickness not more 2.0 mm measured by ultrasound imaging or histopathological examination.

Exclusion criteria

• Subjects who are less than 18 years at the time of informed consent.
• Subject is pregnant or lactating at time of first treatment
• Subjects with extensive, invasive or advanced skin cancer when another method in use such as radiotherapy or Mohs' surgery has priority and offers the patient better opportunity of cure.
• Cancers on anatomical sites where the ultrasound probe cannot be adapted for anatomical reasons
• Any systemic disease that according to investigator's assessment may interfere with the spontaneous course of a skin cancer.
• Any condition predisposing to treatment-related adverse effects or complications from the ultrasound treatment.
• Subjects with abnormal scar formation
• Subjects with impaired wound healing
• Subjects with any other acute or chronic condition which, in the opinion of the investigator, could interfere with the conduct of the study
• Subjects undergoing immunosuppressive treatment

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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27 participants in 1 patient group

De-novo BCC with thickness not more than 2.0 mm

Experimental group

Description:

Areas with de-novo BCC of thickness not more than 2.0 mm (as confirmed by ultrasound imaging or histopathological examination) will be treated by high intensity focused ultrasound

Treatment:

Device: TOOsonix System ONE-M