Clinical Study for Taichi Precise Image
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age23+
SponsorPhilips Clinical & Medical Affairs Global
About this trial
The objective of the study is to evaluate the Image Quality (IQ), and diagnostic acceptability of Precise Image (PI) as compared with iDose4 as a standard-of-care reference. The study is designed to assess the performance of Precise Image algorithm on data collected from subjects scanned by CT Rembra RT, CT Areta RT or CT Rembra. This approach allows for the evaluation of image quality and diagnostic acceptability by comparing the PI algorithm with iDose4, which serves as the standard-of-care reference.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Subjects scanned by CT Rembra RT, CT Areta RT or CT Rembra according to the department standard of care clinical protocols.
Subjects age > twenty-two (22) years
Disqualifiers
Scans that the site radiologists/medical physicists have deemed as non-diagnostic image quality in the standard practice (e.g. patient movement)
Scans that are not completed due to technical difficulties
Trial population
Subjects that are adults over the age of 22 years and scanned by CT Rembra RT, CT Areta RT or CT Rembra.
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
Acceptability of Precise Image reconstruction
The Image Quality and diagnostic acceptability of Precise Image reconstructions are at least as good as (non-inferior to) iDose4 for conventional images.
Time frame
5 months from enrollmentLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
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