Lung Cancer Clinical Trial
Avecure Flexible Microwave Ablation Probe For Lung Nodules
Summary
This research study to determine the effectiveness of the AveCure Flexible Microwave Ablation Probe to destroy cancerous lung nodules up to 3 c m in size.
This research study involves microwave ablation (MWA)
Full Description
This will be a single arm, prospective cohort study.
The names of the study intervention involved in this study is:
Cone Beam Computed Tomography (CBCT)-guided electromagnetic navigational bronchoscopy (ENB) microwave ablation (MWA)
A rapid on-site evaluation (ROSE) will be performed before the MWA to confirm that the lesion is malignant, this can lead to longer procedure time and time under anesthesia.
The research study procedures include screening for eligibility and study treatment including evaluations and follow up visits.
Participants will receive the study intervention and will be followed for 30 days.
It is expected that about 10 people will take part in this research study.
This research study is a Pilot Study, which is the first-time investigators are examining this intervention using a bronchoscopic approach for microwave ablation of solitary pulmonary nodules.
The U.S. Food and Drug Administration (FDA) has approved this intervention as a treatment option for this disease.
Eligibility Criteria
Inclusion Criteria:
Subject with Stage I - II primary lung cancer (Solitary nodules up to 3 cm) as defined by previous pathology or ROSE.
Pathological proof of target nodule/tumor type and malignancy with specimen considered adequate per institutional laboratory standards
Target nodule/tumor which can be accessed via navigational bronchoscopy and confirmed location with cone beam CT scan intra-operatively
Resection/surgical candidate (lobectomy or greater)
Participants must be at least 22 years old and able to provide consent
Exclusion Criteria:
Subjects in whom flexible bronchoscopy is contraindicated
Target nodule < 1.0 cm
Prior radiation or neo adjuvant chemotherapy of the target nodule/tumor
Any comorbidity that the investigator feels would interfere with the safety of the subject or the evaluation of study objectives
Pacemaker, implantable cardioverter, or another electronic implantable device
Patient cannot tolerate bronchoscopy
Patients with coagulopathy
Patients in other therapeutic lung cancer studies
Subject is pregnant or breastfeeding
COVID-19 positive patient at the time of procedure.
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There is 1 Location for this study
Boston Massachusetts, 02115, United States More Info
Principal Investigator
Sub-Investigator
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