ANET Electrosurgery Applicator Pilot Evaluation Study

Status Terminated

Clinical Trial Summary

Evaluate the preliminary safety and performance of the Electrosurgery Applicator (ANET device) during and after bronchoscopic ablation of a target pulmonary nodule/tumor.

Clinical Trial Description

This study is a prospective, single arm, single center study that will evaluate the effectiveness of the ANET Electrosurgery Applicator in up to 10 subjects. Subjects who consent to participate in this study will have a lung tumor that is scheduled to be removed surgically as part of their normal treatment. During the surgical procedure, just prior to resection the subject's tumor will be treated with the ANET device. The ANET device uses a bronchoscope to reach the tumor. Ultrasound on the bronchoscope, CT, and X-rays are used to make sure the ANET device is in the tumor. Once in the tumor, the ANET device uses radio-frequency (RF) ablation to treat the tumor. After standard surgical resection the tumor and surrounding tissue is evaluated to characterize the effect of the ANET. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03400748
Study type	Interventional
Source	Olympus Corporation of the Americas
Contact
Status	Terminated
Phase	N/A
Start date	April 23, 2018
Completion date	November 18, 2020

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