Biograph Vision 600 Versus Biograph Vision.X PET/CT

Valentina Garibotto

Status: Enrolling

Conditions: Alzheimer Disease; Cancer

Treatments: Device: Images

Study type: Interventional

Funder types: Other

Identifiers

NCT07006155

2025-D00005

Details and patient eligibility

About

The main purpose is to evaluate initial clinical experiences and to explore whether the Vision.X system yields improved image quality and diagnostic performance compared to Vision 600.

Enrollment: 40 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Written Inform Consent to participating.
• 18 to 85 years of age
• Willing and able to comply with the requirements of the study, as judged by the investigator

Exclusion criteria

• Women in pregnancy
• Patients unable to lie still for the duration of the examination

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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40 participants in 2 patient groups

Vision X

Experimental group

Description:

PET/CT images acquired with Vision.X

Treatment:

Device: Images

Vision 600

Active Comparator group

Description:

PET/CT images in Vision 600

Treatment:

Device: Images