PET/MRI: PET/MR imaging using an integrated TOF PET/MR scanner (Signa, GE Healthcare, WI, USA)
Study summary
PET/MRI artificial intelligence reconstruction algorithm AIR Recon DL image quality evaluation and clinical study
Eligibility
Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria:
* 1\. Adults between the ages of 18 and 75 who are autonomous; 2. persons with good compliance; 3. those who are mentally alert and able to move around on their own; 4. Those who agree to participate in this clinical trial and sign the informed consent form.
Exclusion Criteria:
* 1\. Persons who do not have full capacity for civil behaviour; 2. Women during pregnancy and breastfeeding; 3. other implants, prostheses, foreign bodies and patches with electronic implants such as pacemakers, insulin pumps and cochlear implants that are not suitable for MRI; 4. patients with claustrophobia; 5. those who, in the opinion of the investigator, are not suitable for participation in this clinical trial.
Primary outcome measure(s)
Signal to Noise Ratio — 1 day from injection of the tracer An important parameter for measuring image quality, indicating the ratio of signal to noise power
Contrast to Noise Ratio — 1 day from injection of the tracer Describes the relative difference in signal strength between the two tissues, the greater the difference the better the image comparison
Trial sites (1)
Facility
City
Region
Status
Department of Nuclear Medicine,Xijing Hospital, Fourth Military Medical University, Xi'an, China, Xi'an, Shaanxi Province
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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