Evaluation of the XACT Robotic System for Image-guided Percutaneous Lung Procedures

Withdrawn before enrolling · Not applicable

Conditions studied: CT-guided Minimally Invasive Procedures e.g. Biopsies

In brief

This is a prospective, single arm study, to evaluate the safety, effectiveness and usability of the XACT device. Subjects undergoing CT-guided, minimally invasive percutaneous lung procedures in the interventional radiology suite. eg. core, biopsy, will participate in the study. System and clinical accuracy will be the primary efficacy endpoint. Usability and safety will also be evaluated.

Key facts

Study ID
NCT04612985
Run by
Xact Robotics Ltd.
People needed
0
Starts
2018-09-01
Expected to finish
2019-12-01
Last updated by the study team
2020-11-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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