A Fast, Quiet, Artificial Intelligence-based PET/MR Solution for Paediatric Diseases
NCT ID: NCT06709690
Last Updated: 2024-11-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
35 participants
OBSERVATIONAL
2024-10-25
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Paediatric patients
Children who have clinical symptoms and are suspected of having malignant tumors after being evaluated by clinical pediatricians and require 18F-FDG PET/MR examination to further clarify their conditions.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Signed and dated informed consent form
3. Commit to complying with the research procedures and cooperate in the implementation of the entire research process.
4. No gender restriction, aged between 0 and 18 years old.
Exclusion Criteria
2. Patients with severe claustrophobia,epileptic seizures, respiratory distress who cannot lie down, and patients with mental anomalies who are unable to cooperate.
3. Patients with metal implants such as pacemakers, artificial metal heart valves, and neurostimulators in their bodies.
4. Non-compliant person.
18 Years
ALL
No
Sponsors
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Ruijin Hospital
OTHER
Responsible Party
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Locations
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China, Shanghai Ruijin Hospital affiliated to Shanghai Jiao Tong University of Medicine
Shanghai, Shanghai Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RuijinH 2024-467
Identifier Type: -
Identifier Source: org_study_id
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