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Research on Alternative Gadolinium Contrast Agents in Dual-Energy CT Imaging Scanning

Prospective Clinical Application Study on Gadolinium Contrast Medium Alternatives in Dual-Energy Imaging of CTA (Computed Tomographic Angiography)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126906
Enrollment
Unknown
Registered
2026-06-18
Start date
2025-10-23
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

1. Atherosclerosis

Interventions

Control group (iodinated contrast medium group)::None
Gadolinium contrast agent group:None

Sponsors

Xi'an Daxing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inclusion Criteria for Gadolinium-Based Contrast Agent Group: (1) Aged 18 years or older; (2) Requiring CTA scanning based on clinical conditions to evaluate one of the following diseases: atherosclerosis, vascular stenosis or occlusion, aortic dissection, pulmonary embolism, and other vascular-related disorders; (3) Patients unsuitable for iodine-based contrast agents due to iodine allergy or severe allergic history, requiring multiple re-examinations after interventional therapy, or renal insufficiency (eGFR 30-60 mL/min/1.73 m^2); (4) Complete imaging data with image quality meeting the minimum diagnostic requirements. 2. Inclusion Criteria for Control Group: (1) Aged 18 years or older; (2) Requiring CTA scanning based on clinical conditions to evaluate one of the following diseases: atherosclerosis, vascular stenosis or occlusion, aortic dissection, pulmonary embolism, and other vascular-related disorders; (3) Complete imaging data with image quality meeting the minimum diagnostic requirements.

Exclusion criteria

Exclusion criteria: 1. Inclusion Criteria for Gadolinium-Based Contrast Agent Group: (1) Aged 18 years or older; (2) Requiring CTA scanning based on clinical conditions to evaluate one of the following diseases: atherosclerosis, vascular stenosis or occlusion, aortic dissection, pulmonary embolism, and other vascular-related disorders; (3) Patients unsuitable for iodine-based contrast agents due to iodine allergy or severe allergic history, requiring multiple re-examinations after interventional therapy, or renal insufficiency (eGFR 30-60 mL/min/1.73 m^2); (4) Complete imaging data with image quality meeting the minimum diagnostic requirements. 2. Exclusion Criteria for Control Group: (1) Known allergy to iodinated contrast media or its components; (2) Severe renal insufficiency (eGFR < 30 mL/min/1.73 m^2); (3) Previously diagnosed nephrogenic systemic fibrosis (NSF); (4) Pregnant or lactating women; (5) Severe cardiopulmonary dysfunction precluding tolerance to scanning; (6) Inability to cooperate with scanning (e.g., severe claustrophobia or failure to remain motionless); (7) Severe neurological disorders (e.g., epilepsy, Parkinson's disease, etc.) that may compromise image quality.

Design outcomes

Primary

MeasureTime frame
Image Quality Assessment;Mean attenuation value of the image;

Secondary

MeasureTime frame
Signal to Noise Ratio;Contrast-to-Noise Ratio;

Countries

China

Contacts

Public ContactYue Qin

Xi'an Daxing Hospital

13363994457@163.com+86 29 8631 0703

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026