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Multi-center clinical controlled study based on 5G remotely-guided CT/MRI scans

A multi-center clinical study on the effect of 5G remote guidance CT/MRI scanning on improving the efficiency and image quality of medical imaging examination

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048271
Enrollment
Unknown
Registered
2021-07-05
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

case series:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for chest CT subjects: (1) Aged 18-60 years; (2) BMI is 18-24 (3) Education level: primary school graduate or above; (4) Those who need to undergo chest CT scan due to the clinical doctor's order; (5) The social function is intact, with full capacity for conduct and responsibility; (6) Voluntarily participate in this study and sign the informed consent. 2. Inclusion criteria for abdominal MRI subjects: (1) Aged 18-60 years; (2) BMI is 18-24; (3) Education level: primary school graduate or above; (4) Abdominal MRI scan is required due to clinical doctor's order; (5) The social function is intact, with full capacity for conduct and responsibility; (6) Voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for chest CT subjects: (1) Those who are unable to hold their breath to cooperate; (2) Those who cannot cooperate (lack of consciousness, irritable patients, etc.); (3) Critically ill patients; (4) Those who have recently planned to conceive or are already pregnant. 2. Exclusion criteria for abdominal MRI subjects: (1) Those with metal foreign bodies (such as pacemakers, cochlear implants, etc.) in the body; (2) Critically ill patients with non-MRI compatible ventilator and ECG monitoring equipment; (3) Those who have neurostimulators such as insulin pumps; (4) Early pregnant women within three months of pregnancy; (5) Those who are unable to hold their breath to cooperate; (6) The claustrophobic.

Design outcomes

Primary

MeasureTime frame
image quality;disgnostic accuracy;scanning time;

Countries

China

Contacts

Public ContactLi Zhenlin

West China Hospital of Sichuan University

HX_lizhenlin@126.com+86 18989602130

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026