Precise Image for Interventional CT

NCT ID: NCT07317427

Last Updated: 2026-01-05

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

55 participants

Study Classification

OBSERVATIONAL

Study Start Date

2026-01-31

Study Completion Date

2026-10-01

Brief Summary

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The purpose of this clinical study is to assess the performance of the Precise Image reconstruction algorithm on interventional CT images acquired from adult patients (\>18 years old). The analysis will focus on the performance of Precise Image for scans in which procedural instruments (e.g., needle, probe, screw) are present. Clinical data generated from this study is intended to support a proposed expansion of the Indications for Use of Precise Image.

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.

Detailed Description

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Conditions

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Computed Tomography

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Subjects scanned by FDA-cleared and marketed Philips Incisive CT or CT 5300 systems, and according to the department standard of care clinical protocols for the applicable clinical scans.
* Subject age: \>18 years old.
* Presence of procedural instrument(s) (e.g., needle, probe, screw) in the CT images.

Exclusion Criteria

* Subject age: 18 years old and below.
* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Philips Healthcare (Suzhou) Co., Ltd.

INDUSTRY

Sponsor Role collaborator

Philips Clinical & Medical Affairs Global

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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Precise Image for CCT

Identifier Type: -

Identifier Source: org_study_id

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