Computed TomographyNCT07317427
Precise Image for Interventional CT
An observational study of Computed Tomography, run by Philips Clinical & Medical Affairs Global.
Trial summary
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). Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Computed Tomography
- How many people
- 55 participants
- Where
- No sites listed yet
- Study dates
- 31 Jan 2027to 1 Dec 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 19 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adults
Who may be able to join
- 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.
Who cannot join
- 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.
- Scans that the site interventional radiologists have deemed non-suitable for procedural guidance.
About this study
Official title: Clinical Study for Precise Image for Interventional CT for Incisive CT and CT 5300 Systems
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:
Read more
- To evaluate the image quality for procedural guidance of Precise Image compared to the standard-of-care reference (iDose4) for:
- Interventional CT images of adult patients (>18 years old).
- To demonstrate non-inferiority of Precise Image to iDose4 for the relevant interventional CT images.
- Conditions
- Computed Tomography
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of the CT image quality of Precise Image reconstructions via a 5-point Likert Scale
The image quality of Precise Image reconstructions will be considered at least as good as (non-inferior to) that of iDose4 reconstructions for interventional CT images (CCT single, continuous, fluoro) of adult patients (>18 years old)
Measured: Reading session at 4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jan 2026
- Study start31 Jan 2027 (estimated)
- Primary completion1 Jun 2027 (estimated)
- Study completion1 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Computed TomographyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 55 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Philips Clinical & Medical Affairs Global
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Philips Healthcare (Suzhou) Co., Ltd.
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07317427
- Sponsor's protocol ID
- SEF-2025-301308
- Status last verified
- Aug 2026
- First submitted
- 23 Sep 2025
- Last updated
- 25 Aug 2026
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Study for Precise Image for Interventional CT for Incisive CT and CT 5300 Systems
- ClinicalTrials.gov ID
- NCT07317427
- Acronym / sponsor ID
- SEF-2025-301308
- Conditions
- Computed Tomography
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 55 participants (estimated)
- Lead sponsor
- Philips Clinical & Medical Affairs GlobalIndustry (pharma, biotech, devices)
- Collaborators
- Philips Healthcare (Suzhou) Co., Ltd.
- Study start
- 31 Jan 2027 (estimated)
- Primary completion
- 1 Jun 2027 (estimated)
- Study completion
- 1 Dec 2027 (estimated)
- First posted
- 5 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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:
- To evaluate the image quality for procedural guidance of Precise Image compared to the standard-of-care reference (iDose4) for:
- Interventional CT images of adult patients (>18 years old).
- To demonstrate non-inferiority of Precise Image to iDose4 for the relevant interventional CT images.
Study design
- Observational model
- Other
- Time perspective
- Retrospective
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adults
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (5 listed)
- 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.
- Scans that the site interventional radiologists have deemed non-suitable for procedural guidance.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Assessment of the CT image quality of Precise Image reconstructions via a 5-point Likert Scale
Time frame: Reading session at 4 months
The image quality of Precise Image reconstructions will be considered at least as good as (non-inferior to) that of iDose4 reconstructions for interventional CT images (CCT single, continuous, fluoro) of adult patients (>18 years old)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Aug 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Computed Tomography, run by Philips Clinical & Medical Affairs Global.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 25 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assessment of the CT image quality of Precise Image reconstructions via a 5-point Likert Scale (time frame: Reading session at 4 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Aug 2026.