Health TrialsbyHealthPanel

XACT ACE Observational Registry

ConditionTumors
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorXact Robotics Ltd.

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

≥ 18 years of age

Subjects undergoing CT-guided, minimally invasive percutaneous procedures in the interventional radiology suite

Subject is willing to sign informed consent for the purposes of data collection

Disqualifiers

None

Trial population

Subjects undergoing CT guided, minimally invasive percutaneous procedures in an interventional radiology setting.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

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

    Device

    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.

Treatment groups

500 Participants
are divided into 1 treatment group
Group A: All subjects1 intervention

Trial outcomes

Primary outcomes

1

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
2

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
3

Assessment of Safety

Incidence of intra- and post-procedural events

Time frame
2 hours post-procedure

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Xact Robotics Ltd.

Lead sponsor

Source ClinicalTrials.gov
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