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A Prospective, Single-center, Diagnostic Efficacy and Safety Verification Clinical Trial based on NAEOTOM Alpha.Pro Photon-counting CT

A Prospective, Single-center, Diagnostic Efficacy and Safety Verification Clinical Trial based on NAEOTOM Alpha.Pro Photon-counting CT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113076
Enrollment
Unknown
Registered
2025-11-24
Start date
2025-11-25
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

None

Interventions

Observation group:NA

Sponsors

Beijing Chao-Yang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age: 18 to 75 years old; 2) Those who agree to participate in this clinical trial and sign the informed consent form for subjects; 3) Where the woman agrees to contraception and the man agrees to contraception with his partner; 4) Negative pregnancy test results for women of childbearing age.

Exclusion criteria

Exclusion criteria: 1.Satisfying any one of these conditions will rule out: 1)A person without full capacity for civil conduct. 2) The pregnancy test of women of childbearing age is positive. 3) Lactating women. 4) Those who the researcher deems unsuitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Overall image quality excellence rate;

Secondary

MeasureTime frame
Image Quality Comparison Excellence Rate;

Countries

China

Contacts

Public ContactQi Yang

Beijing Chao-Yang Hospital, Capital Medical University

yangyangqiqi@gmail.com+86 189 1076 6178

Outcome results

None listed

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