Precise 3D Surview
ConditionComputed Tomography
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPhilips Clinical & Medical Affairs Global
About this trial
The purpose of the study is to assess the performance of Precise 3D Surview on CT 5300 and Incisive CT Scanners as compared with manual annotation by experienced CT technologists.
* To evaluate the acceptance rate of the Auto 3D Planning Box compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of the Auto Suggestion for Locator compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of the Auto Planning for Truncated Anatomies (lung and liver) compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of Auto Planning and Symmetry Correction for Tilted Head compared with manual annotation by experienced CT technologists.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Subjects scanned by CT 5300 (K232491) and Incisive CT (K212441) according to the department standard of care clinical protocols.
Subjects age is over eighteen (18) years1.
Patients scanned in supine orientation.
Non-contrast CT scan
Disqualifiers
Subjects age is under or equal 18 years old
Patients are not scanned in supine orientation.
Contrast-enhanced CT scans.
CT scans with high resolution
Trial population
Adults
Trial design
Design model
Other
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Acceptance rate of the 3D Surview
Time frame
Reading session at 4 monthsLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Philips Clinical & Medical Affairs Global
Lead sponsor
Philips Healthcare (Suzhou) Co., Ltd.
Collaborator
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: