Topic: Surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Willing and able to give informed consent 2. Aged 18 or over 3. Booked for an X-ray guided intervention in an anatomic zone covered by the technology (currently paravertebral: e.g. aortoiliac, spinal, retroperitoneal, pelvic) 4. Have had a preoperative CT scan 5. Able (in the investigator's opinion) and willing to comply with the study requirements
Exclusion criteria
Exclusion criteria: 1. Female participants who are pregnant or planning pregnancy during the course of the study 2. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant’s ability to participate in the study 3. Participants who have participated in another research study involving an investigational product in the past 12 weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Accuracy and robustness; Timepoint(s): Real-time acquisition of image registration data during X-ray guided procedure for analysis | — |
Secondary
| Measure | Time frame |
|---|---|
| Measured once during the X-ray guided intervention: 1. Procedure time 2. Radiation dose 3. Iodinated contrast dose | — |
Countries
United Kingdom