About this trial
The study is going to enroll about 220 consecutive patients with screws in lumber spine after internal fixation surgery who underwent follow-up assessment using Incisive CT according to the department standard of care. Retrospective data sets will be reconstructed into conventional image, the O-MAR algorithm, and Precise-MAR. Three blinded, independent radiologists evaluate both qualitative and quantitative analysis of image quality of surrounding tissue and artifact. Statistical analysis included the Friedman test, Wilcoxon signed-rank test, and Levene test.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Images come from patients aged ≥ 18 years,
Images come from patients with screws in lumber spine after internal fixation surgery underwent follow up Incisive CT scan;
Images come from patients who comply with the requirements of informed consent at the study site.
Disqualifiers
Patients with other metal objects inside or outside the body
There is movement during the CT scan, causing by breathing etc. artifact affecting image quality
Data is considered unsuitable for enrollment based on the investigator's evaluation due to incomplete clinical data or radiological information etc.
Trial population
The study participants from Beijing Jishuitan Hospital.
Trial design
Case-only
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Image Quality-4 Likert Scale
The radiologist will evaluate the image quality using Likert scale on a scale ranging from 0(poor) to 4(good)
Locations
Sponsors and contacts
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Philips Clinical & Medical Affairs Global
Lead sponsor
Beijing Jishuitan Hospital
Collaborator
This trial is not recruiting at the moment. You can still explore other options: