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RecruitingObservational

Observational Post-Market Study of the XACT ACE Robotic System

NCT ID: NCT04950959Sponsor: Xact Robotics Ltd.Last updated: 2022-10-21

Summary

Compile real world data on the use of the XACT ACE Robotic System

Detailed description

The purpose of this observational post-market study is to compile real world data on the use of the XACT ACE Robotic System in subjects undergoing CT guided, minimally invasive percutaneous procedures. The objectives are to 1) evaluate the proportion of procedures in which the instrument reached the pre-defined target, based on the physician's determination and CT imaging confirmation, 2) To evaluate system accuracy defined as the measured distance from the tip of the instrument to the target location at the at the end of the instrument insertion, and 3) Incidence of intra- and post-procedural adverse events. Up to 500 patients will be enrolled in this multicenter, nonrandomized, single arm registry.

Arms & interventions

  • DeviceHands-free, user-controlled robotic system intended to assist in the planning and advancement of an instrument during CT guided percutaneous procedures. T

    The system is used for trajectory planning and is intended to assist the physician in the positioning of an instrument, such as a needle, where CT imaging is used for target trajectory planning and intraoperative tracking. The XACT ACE Robotic System uses a computerized quantitative guidance system, which provides real-time, accurate needle guidance, including advancement and steering of the needle from the entry point on the subject's body to the target point within the body.

Outcome measures

Primary

  • Proportion of successful procedures

    To evaluate the proportion of procedures in which the instrument reached the pre-defined target based on the physician's determination and CT imaging confirmation.

    Time frame: 1 hour

  • System accuracy

    To evaluate system accuracy defined as the measured distance from the tip of the instrument to the target location at the end of the instrument insertion.

    Time frame: 1 hour

  • Assessment of Safety

    Incidence of intra- and post-procedural events

    Time frame: 2 hours post-procedure

Eligibility criteria

Sex: AllAge: 18 Years and older
Inclusion Criteria: 1. ≥ 18 years of age 2. Subjects undergoing CT-guided, minimally invasive percutaneous procedures in the interventional radiology suite 3. Subject is willing to sign informed consent for the purposes of data collection Exclusion Criteria: 1\. No exclusion criteria other than listed in the product Instructions for Use (IFU)

Study locations (1)

Lahey Hospital and Medical Center

Burlington, Massachusetts, 01805

Recruiting
Nanette Matrullo · Contact
Sebastian Flacke, MD · Principal Investigator
XACT ACE Observational Registry | Cancerify