Actively Recruiting

Age: 18Years - 89Years
All Genders
NCT06691659

Next-Generation Photon-Counting CT Technology: Development and Clinical Evaluation

Led by University of Pennsylvania · Updated on 2025-10-14

250

Participants Needed

1

Research Sites

105 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

C

Canon Medical Systems, USA

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project aims to develop and evaluate a next-generation photon-counting CT prototype, and assess whether next-generation photon-counting CT--which enables reduced radiation dose, high spatial resolution, and spectral imaging--would facilitate improved diagnostic performance for abdominal, cardiothoracic, musculoskeletal, and neuroimaging.

CONDITIONS

Official Title

Next-Generation Photon-Counting CT Technology: Development and Clinical Evaluation

Who Can Participate

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 89 years
  • Participants must be informed of the investigational nature of this study and be willing to provide written informed consent
  • Participants must agree to participate according to institutional and federal guidelines
  • Not pregnant (based on attestation)
Not Eligible

You will not qualify if you...

  • Pregnant women are excluded; females of childbearing potential must confirm they are not pregnant before CT imaging
  • Known allergy to contrast agents
  • Any current medical condition or illness that could compromise safety or successful participation, as determined by a physician

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania - Center for Advanced Computed Tomography Imaging Services (CACTIS)

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

E

Erin Schubert

CONTACT

H

Hannah Straughn

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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