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CompletedNCT06589934Updated Nov 25, 2025

Clinical Study of CT 5400 RT for Precise Image Validation

An interventional study of Precise Image in Precise Image (AI Reconstruction Feature of CT 5400 RT System), sponsored by Philips Clinical & Medical Affairs Global. Completed at 1 site in China. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-25.

Sponsored by Philips Clinical & Medical Affairs Global · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the effectiveness of the Precise Image (PI), an AI feature of CT 5400 RT System

02

Conditions studied

  • Precise Image (AI Reconstruction Feature of CT 5400 RT System)
03

In context

Lead sponsor

Philips Clinical & Medical Affairs Global is the lead sponsor of 82 studies on the registry; 24 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 10 (77%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 30 image raw data generated from CT 5400 RT system validation clinical trial (protocol name: Clinical study of CT 5400 RT for system validation, ClinicalTrials.gov ID: NCT06466577)
  • Applicable body parts include: head, neck, chest, abdomen and coronary

Exclusion criteria

Exclusion Criteria:

  • Raw data is considered inappropriate for inclusion
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Image quality

    Diagnostic Test -Good and excellent rate of PI image quality is greater than or equal to 95%. PI image quality will be assessed by using the retrospective image raw data obtained from CT 5400 RT (applicable body parts include: head, neck, chest, abdomen and coronary)

    Diagnostic Test: Precise Image

Interventions

  • Diagnostic testPrecise Image

    Image reconstruction software

06

What researchers measure

Primary outcomes

  1. Clinical image quality(IQ)

    Image quality will be assessed by Likert score (1-5)

    Time frame: 14 days (anticipated)

07

Study locations

1 site
  • Shanghai Public Health Clinical Center
    Shanghai, Shanghai Municipality 200120, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06589934
Lead sponsor
Philips Clinical & Medical Affairs Global
Collaborators
Philips Healthcare (Suzhou) Co., Ltd.
Responsible party
Sponsor
First posted
Sep 19, 2024
Start date
Jan 25, 2025
Primary completion
Jan 25, 2025
Completion
Mar 25, 2025
Last update
Nov 25, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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