Intra-individual patient-based comparison of conventional and digital PET/CT scanners

• Conditions: cancer; oncology; 10027655

• Registration Number: NL-OMON46943
• Lead Sponsor: Isala, Zwolle

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 225

Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria:
* referred for a clinically indicated FDG-PET/CT scan
* suspected or proven lung cancer, breast cancer and a group of miscellaneous cancers
* signed informed consent

Exclusion Criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study:
* age < 18 years
* incapacitated adults
* prisoners
* pregnant woman
* not able to undergo two consecutive PET/CT scans

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Final result of the PET/CT study. This outcome parameter includes multiple<br /><br>parameters, such as the number of regional lymph nodes, the number of distant<br /><br>metastasis and the final TNM classification.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>PET image quality. This outcome parameter includes multiple parameters, such as<br /><br>the image noise, diagnostic confidence and lesion detectability<br /><br>(contrast-to-noise etc.).</p><br>