Ultrasound-CT Fusion System for Interventional Radiology Procedures

Not Applicable

• Conditions: CT Guided Drain Placement Within the Abdomen or Pelvis; CT Guided Biopsy; CT Guided Injection of Muscle or Nerve Within the Pelvis
• Interventions: Device: Ultrasound-CT Fusion

• Registration Number: NCT03226535
• Lead Sponsor: Clear Guide Medical

Brief Summary

The objective of this research is to use the Clear Guide SCENERGY technology, an FDA approved Ultrasound-CT fusion imaging system, that allows the user to fuse CT images onto a real-time ultrasound that is being performed on the patient. This fusion system will be used to perform ultrasound guided needle placements for patients undergoing percutaneous CT guided needle-based intervention. This study will consist of 20 patients, 10 patients using the CGM SCENERGY US-CT system and 10 patients using guidance only. The primary goal of the study is to prove that the new imaging fusion system is comparable to using either CT or US guidance alone to guide needle placement.

Detailed Description

A simple 20 patient study will be performed using the CG SCENERGY system. This fusion system will be used to perform image guided needle placements for patients undergoing percutaneous CT guided needle-based intervention (CT guided biopsy, CT guided drain placement within the abdomen or pelvis, and CT guided injection of muscle or nerve within the pelvis). Only patients who are already scheduled for a CT guided procedure will be screened. The study design is as follows:

* 10 patients will have their procedure performed using the CGM SCENERGY US-CT fusion system and 10 patients will have their procedure performed using CT guidance only.

* Proper informed consent will be obtained

* Perform a CT scan with the optical adhesive skin markers in place. Markers are placed around the expected site of needle skin entry.

* The first 10 patients Group#1 (1-10) will be assigned to using the SCENERGY fusion system to complete the needle placement, and the next 10 patients Group #2 (11-20) will be assigned of continuing with CT guidance only to complete the needle placement.

* If in Group #1, the procedure will proceed as usual using the SCENERGY system to guide the needle to target. If in the Group #2, CT guidance will be used to place the needle to target.

* Once the needle is at the target, a confirmatory CT will be performed.

* If the target is reached (i.e., the software directed the interventional radiologist to the right place, e.g. for correctly biopsying a lesion), the trial is considered a "success" and the procedure continues as normal.

* If the needle is not in the right place, the trial is considered a "failure", and the procedure continues as normal without using the CGM software any further.

Study Timeline

• Study Start: 2017-06-22
• Status Verified: 2017-07
• Study First Submitted: 2017-07-18
• Study First Submitted QC: 2017-07-20
• Last Update Submitted: 2017-07-20
• Study First Posted: 2017-07-21
• Last Update Posted: 2017-07-21
• Primary Completion: 2018-06-22
• Study Completion: 2018-06-22

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Undergoing percutaneous CT guided needle-based intervention (CT guided biopsy, CT guided drain placement within the abdomen or pelvis, and CT guided injection of muscle or nerve within the pelvis)
• Able to give written informed consent

Exclusion Criteria

• Unable to give informed consent
• Patients undergoing CT guided needle-based interventions other than the procedures mentioned in the inclusion criteria
• Prisoners, pregnant women, and children

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Ultrasound-CT Fusion Guidance	Ultrasound-CT Fusion	The participants in this group (test group) will utilize the ultrasound-CT fusion system for guiding needle placement.

Primary Outcome Measures

Name	Time	Method
Number of CT scans or CT fluoroscopic images	Immediately following intervention (within 2 hours)

Secondary Outcome Measures

Name	Time	Method
Total procedure time	Immediately following intervention (within 2 hours)	Time from the first CT scan until the needle is at the target
Time to target	Immediately following intervention (within 2 hours)	Time from needle entering the skin until the needle is at the target
Success of needle placement	Immediately following intervention (within 2 hours)	A confirmatory CT will be performed to check if the needle reached the target

Trial Locations

Locations (1)

Johns Hopkins Hospital; 🇺🇸 Baltimore, Maryland, United States