A Study of a New PET Scanner in People With Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The researchers are doing this study to test the capabilities of a new total-body PET scanner called the Biograph Vision Quadra. The researchers want to learn whether this scanner can produce better PET/CT images and provide more useful imaging information than standard PET/CT scanners.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with histologically-confirmed non-small cell lung carcinoma (NSCLC) with a single or multiple lung nodules.

Patients who are undergoing a planned PET-CT scan at main campus of MSK.

Patients must be ≥ 18 years old

Patients with disease within the chest, abdomen or pelvis, who could benefit from visualizing the pharmacokinetics of radiotracer uptake within all disease sites simultaneously.

Disqualifiers

Patients who suffer from claustrophobia.

Women who are pregnant or breast-feeding.

Patients < 18 years of age

Trial population

Any MSKCC patients with histologically confirmed cancer, who will be scheduled to receive a planned PET-CT scan at the MSK main campus may be enrolled in this image evaluation and improvement study. Potential patients will be identified by a member of the patient's treatment team at MSKCC, who will introduce the study to them.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Biograph Vision Quadra scanner

    Diagnostic test

    new total-body PET scanner, 1 or 2 additional scans with the Biograph Vision Quadra scanner.

  • PET/CT

    Diagnostic test

    Scheduled PET/CT scan

Treatment groups

90 Participants
are divided into 1 treatment group
Group A: Patients with lung, head and neck, and prostate cancer2 interventions

Trial outcomes

Primary outcomes

1

image quality

Detection of any new/additional lesions on the delayed scan will be recorded using standard clinical interpretation.

Time frame
3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.