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
120 participants
OBSERVATIONAL
2026-01-31
2026-10-01
Brief Summary
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The study has two objectives:
1. To evaluate the extent of metal artifacts and diagnostic confidence, and overall image quality (independent of metal artifacts) of P-MAR compared to images without metal correction, and compared to O-MAR, for CT images (with metal present) of adult patients (\>18 years old).
2. To demonstrate non-inferiority of P-MAR compared to images without metal correction for the relevant metal groups.
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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: Above 18 years old.
* Scans with metal present (orthopedic implants/joint prothesis, dental filling/implants, spine screw(s), pacemaker, coils, radiotherapy beads, surgical clips/staples, metal objects either outside the body or near air, etc.)
Exclusion Criteria
* CT scans with no metal present.
* CT scans with metal with motion artifacts.
* Surview or Locator/Tracker.
* CT scans performed utilizing respiratory gating (e.g., "pulmo gating").
* CT scans performed utilizing cardiac gating.
* CT Perfusion scans.
* CCT scans.
* Scans that the site radiologists have deemed as non-diagnostic image quality in standard practice (e.g. patient movement).
* Scans that are not completed due to technical difficulties.
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 MAR
Identifier Type: -
Identifier Source: org_study_id
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