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NCT Number: NCT07759011

Clinical Study of Spectral CT Verida

This study will prospective enroll 80 subjects to evaluate the comparison of image quality, proportion of high-quality images, and image noise between the Spectral Precise Image (SPI) intelligent denoising for low-dose scans on the Spectral CT Verida system and iDose4 reconstructions after low-dose and routine-dose scans.

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Key information

Conditions

Volunteers

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 ≤ age ≤ 75 years.
  • 18 kg/m² ≤ BMI ≤ 28 kg/m².
  • Conscious, able to cooperate, and competent to perform study procedures. Voluntarily agrees to participate in this clinical study and has signed the informed consent form.
  • Women of childbearing potential must have a negative pregnancy test and have no plans to become pregnant during the next 6 months.

Exclusion criteria

  • Persons without full civil capacity.
  • Pregnant or breastfeeding women.
  • Any other conditions that, in the investigator's judgment, make the subject unsuitable for participation in this clinical study.

Treatment and study plan

CT Radiation Scan

Radiation

Use investigated CT do radiation scan

Primary outcomes

  1. The rate of good-excellent scores ≥3

    Time frame: From date of image reconstruction until the date of image reading completion, anticipated 1Week.

    Image quality will be assessed by 2 radiologists using Likert-scale on a range from 1(poor) to 5(Excellent),and calculate the rate of ≥3 with FAS,PSS SS as the datasets analysis.

Secondary outcomes

  1. Objective outcome:Image Noise

    Time frame: From Image reconstruction to image noise recording finished，estimate 1Week.

    Will use FAS,PSS,SS do the image noise (parameters record)datasets analysis.

Study contacts

Contact information is provided by the study sponsor or research team.

Yu De Xin

CONTACT

[email protected]

+8618560081629

Sponsors and collaborators

Lead sponsor

Philips Clinical & Medical Affairs Global

Industry

Collaborators

  • Qilu Hospital of Shandong University

Registry information

Official study title

Prospective, Single-Center Evaluation of Image Quality for Low-Dose Scans With Spectral Precise Image (SPI) Intelligent Denoising Versus iDose4 Reconstructions for Low- and Standard-Dose Scans - Clinical Study Protocol

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Aug 11, 2026
Registry last updated
Aug 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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