Magnetic Resonance-Guided Laser Interstitial Thermal Therapy for Brain Metastases Trial

Capital Medical University

Status: Completed

Conditions: Brain Metastasases

Treatments: Device: Laser interstitial thermal therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT07132203

QX2021-025-02

Details and patient eligibility

About

In accordance with the requirements of the "Good Clinical Practice for Medical Devices", this clinical trial is conducted to further evaluate the safety and efficacy of the magnetic resonance-guided laser ablation treatment system and the laser ablation minimally invasive treatment kit produced by Sinovation (Beijing) Medical Technology. This clinical trial adopts a multi-center, single-groupdesign. After all subjects sign the informed consent form and pass the screening, they will receive the implantation and treatment of the trial products. Follow-up visits will be conducted on the 2±1 day after the surgery, and the efficacy rate of ablation as assessed after the surgery was used as the primary outcome.

Enrollment: 98 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age 18 years and above;
2. Previously diagnosed or newly diagnosed with a malignant tumor in the body accompanied by intracranial metastasis;
3. The lesion can be clearly identified in the magnetic resonance imaging, and the number of lesions does not exceed 4;
4. The lesion to be treated by ablation has a short axis of ≤ 30mm;
5. Karnofsky Performance Status (KPS) score ≥ 60;
6. The subject or their guardian can understand the purpose of the trial, demonstrate sufficient compliance with the trial protocol, and sign the informed consent form.

Exclusion criteria

1. Patients with contraindications for MRI;
2. Patients with severe coagulation dysfunction;
3. Pregnant or lactating women, and those planning to conceive within 6 months;
4. Patients with the longest axis of the maximum brain metastasis lesion less than 5mm;
5. Subjects who have participated in any clinical trials of drugs or medical devices within 3 months before screening;
6. Patients judged by the researcher to be unable to tolerate ablation treatment;
7. Patients judged by the researcher to have evidence of severe or uncontrollable systemic diseases;
8. Subjects considered by the researcher to be unsuitable for this clinical trial.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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98 participants in 1 patient group

laser interstitial thermal therapy

Experimental group

Description:

The subjects will undergo laser interstitial thermotherapy after the screening process is completed. There will be no restrictions on other treatment methods.

Treatment:

Device: Laser interstitial thermal therapy