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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON46943

Enrollment

225

Registered

2018-02-27

Start date

2017-11-13

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cancer oncology

Interventions

not applicable

oncology

PET/CT

staging

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

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

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: * age

Design outcomes

Primary

Measure	Time frame
Final result of the PET/CT study. This outcome parameter includes multiple parameters, such as the number of regional lymph nodes, the number of distant metastasis and the final TNM classification.	—

Secondary

Measure	Time frame
PET image quality. This outcome parameter includes multiple parameters, such as the image noise, diagnostic confidence and lesion detectability (contrast-to-noise etc.).	—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)