HumRes66666
|
SNCTP000006355
|
BASEC2025-D0005
Intra-individual comparison of images from the PET/CT Biograph Vision 600 with the new PET/CT Biograph Vision.X
Summary description of the study
The Nuclear Medicine and Molecular Imaging department has acquired a new instrument, and we would like to compare the image quality of the new instrument with the quality of the instrument we have had for several years.
(BASEC)
Intervention under investigation
PET/CT
(BASEC)
Disease under investigation
cancer
(BASEC)
Criteria for participation in trial
- Written consent - Aged 18 to 85 - Willingness and ability to comply with the study requirements (BASEC)
Exclusion criteria
- Pregnant women - Patients unable to remain still during the examination (BASEC)
- Written consent - Aged 18 to 85 - Willingness and ability to comply with the study requirements (BASEC)
Exclusion criteria
- Pregnant women - Patients unable to remain still during the examination (BASEC)
Trial sites
Geneva
(BASEC)
not available
Sponsor
Hôpitaux Universitaires de Genève
(BASEC)
Contact
Contact Person Switzerland
Pre Valentina Garibotto
+41 22 372 72 52
valentina.garibotto@clutterhug.chHUG
(BASEC)
Scientific Information
not available
Name of the authorising ethics committee (for multicentre studies, only the lead committee)
Ethics Committee Geneva
(BASEC)
Date of authorisation
08.04.2025
(BASEC)
ICTRP Trial ID
not available
Official title (approved by ethics committee)
Intra-individual comparison of PET scans on the Biograph Vision 600 with the new Biograph Vision.X PET/CT (BASEC)
Academic title
not available
Public title
not available
Disease under investigation
not available
Intervention under investigation
not available
Type of trial
not available
Trial design
not available
Inclusion/Exclusion criteria
not available
not available
Primary and secondary end points
not available
not available
Registration date
not available
Incorporation of the first participant
not available
Secondary sponsors
not available
Additional contacts
not available
Secondary trial IDs
not available
Results-Individual Participant Data (IPD)
not available
Further information on the trial
not available
Results of the trial
Results summary
not available
Link to the results in the primary register
not available