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Dual-Source Dual-Wide-Body High-Definition CT System Clinical Trial

Dual-Source Dual-Wide-Body High-Definition CT System Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118148
Enrollment
Unknown
Registered
2026-02-02
Start date
2026-02-08
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

None

Interventions

Sponsors

Zhongshan Hospital,Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years; 2. Agree to participate in this clinical trial and sign the informed consent form; 3. Have full legal capacity.

Exclusion criteria

Exclusion criteria: 1. Individuals without full civil capacity; 2. Women who are pregnant or breastfeeding; 3. High-risk groups with contraindications or allergies to iodine contrast agents (exclusion required only for enhanced scans); 4. Individuals with renal dysfunction (exclusion required only for enhanced scans); 5. Those whom the researchers deem unsuitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Clinical image quality acceptance rate;

Secondary

MeasureTime frame
Incidence of adverse events and serious adverse events;

Countries

China

Contacts

Public ContactMengsu Zeng

Zhongshan Hospital, Fudan University

zeng.mengsu@zs-hospital.sh.cn+86 21 6404 1990

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026