Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
55 participants
OBSERVATIONAL
2026-01-31
2026-10-01
Brief Summary
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The study has two objectives:
1. To evaluate the image quality for procedural guidance and procedural confidence of Precise Image compared to the standard-of-care reference (iDose4) for:
* Interventional CT images of adult patients (\>18 years old).
2. To demonstrate non-inferiority of Precise Image to iDose4 for the relevant interventional CT images.
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Detailed Description
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Conditions
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Study Design
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OTHER
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Subject age: \>18 years old.
* Presence of procedural instrument(s) (e.g., needle, probe, screw) in the CT images.
Exclusion Criteria
* Absence of procedural instrument(s) (e.g., needle, probe, screw) in the CT images.
* Scans that were acquired using a kilovoltage peak of 70 kVp (as Precise Image does not support a kilovoltage peak lower than 80 kVp).
* Scans that the site interventional radiologists have deemed non-suitable for procedural guidance.
18 Years
ALL
No
Sponsors
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Philips Healthcare (Suzhou) Co., Ltd.
INDUSTRY
Philips Clinical & Medical Affairs Global
INDUSTRY
Responsible Party
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Other Identifiers
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Precise Image for CCT
Identifier Type: -
Identifier Source: org_study_id
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