EPIONE Guided Lung Evaluation

Sponsor
Quantum Surgical
Study ID
NCT05651867
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • EPIONE device — DEVICE
    The EPIONE device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography (CT) guided percutaneous procedures.

Study Details

Interventional clinical study to obtain performance and safety data of the EPIONE® device when used for percutaneous procedures in the lung.

Key Dates

Start date
Nov 28, 2022
Status verified
Jun 2025
Primary completion
Aug 25, 2023
Completion
Sep 10, 2024

Study Design

Enrollment
25 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Interventional arm
    Patients treated by percutaneous CT-guided procedures in the lung with the EPIONE® device

Primary Outcome Measure

Feasibility of the Device [ Time Frame: an average of 7 months ]

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