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Spectral CT Clinical Trial Protocol

Spectral CT Clinical Trial Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049948
Enrollment
Unknown
Registered
2021-08-14
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

N\A

Interventions

case series:Breast CT scan

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Volunteers are between 18 and 75 years old; 2. Women of childbearing age have a negative pregnancy test; 3. Those who agree to participate in this clinical trial and sign the subject's informed consent; 4. Enhanced scan requires laboratory tests to prove normal renal function.

Exclusion criteria

Exclusion criteria: 1. Women who are breastfeeding; 2. People who are not suitable for enhanced scanning with iodine contrast agent; 3. Patients who are considered by the investigator to be inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Excellent and good rate of clinical imaging;

Secondary

MeasureTime frame
Common functions, easy to use and satisfaction with the function and stability of the whole machine;Adverse events and serious adverse events;

Countries

China

Contacts

Public ContactLiu Shiyuan

Shanghai Changzheng Hospital

cjr.liuhiyuan@vip.163.com+86 13761304518

Outcome results

None listed

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