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Clinical investigation of uCT 550 guided interventional procedure

Clinical investigation of uCT 550 guided interventional procedure

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074913
Enrollment
Unknown
Registered
2023-08-21
Start date
2023-08-21
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

tumour

Interventions

Sponsors

Zhongshan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age 18 to 75 years; Patients with full capacity for civil conduct; After the analysis of imaging results, the clinical diagnosis is still not possible, and interventional procedure must be performed; Patients who voluntarily participate in this clinical trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Patients who do not have full capacity for civil conduct; pregnant and lactating women; Patients who wish to have children within the next 6 months; Patients with contraindications to anesthesia; Patients that the investigator believes not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Effectiveness of images;

Secondary

MeasureTime frame
Interaction convenience, reliability and safety of the function;

Countries

China

Contacts

Public ContactMengsu Zeng

Zhongshan Hospital Affiliated to Fudan University

zeng.mengsu@zs-hospital.sh.cn+86 21610773

Outcome results

None listed

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