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Double low dose study of dynamic scanning with diluted iso-osmolar contrast medium in head and neck dual-source CT angiography: a self-controlled study

Double low dose study of dynamic scanning with diluted iso-osmolar contrast medium in head and neck dual-source CT angiography: a self-controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041502
Enrollment
Unknown
Registered
2020-12-27
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

Cerebral and carotid artery disease

Interventions

Double low dose group:Double low dose study of dynamic scanning with diluted iso-osmolar contrast medium in head and neck CT angiography
Conventional dose group:Routine head and neck CTA, no low-dose examination

Sponsors

Changzhou Wujin People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-80 years. 2. Patients with BMI < 30 kg / m2. 3. Patients with suspected or confirmed head and neck artery disease. 4. For patients with subarachnoid hemorrhage and intracranial aneurysm found by CTA, CTA was reexamined 7-14 days after onset to observe whether there was cerebral vasospasm 5. The patients who volunteered to join the study signed the informed consent form and had good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to iodine containing contrast media. 2. Patients with severe hyperthyroidism, renal insufficiency and decompensated cardiac insufficiency. 3. Patients with obvious moving artifacts. 4. Patients with failed angiography.

Design outcomes

Primary

MeasureTime frame
CT value of blood vessel;

Secondary

MeasureTime frame
Signal-to-Noise Ratio, SNR;Contrast-to-Noise Ratio, CNR;body Mass Index, BMI;total amount of intake of contrast medium;radiation dose;venous contamination;image quality (subjective evaluation);

Countries

China

Contacts

Public ContactWu Honglin

Changzhou Wujin People's Hospital

wuhljs@163.com+86 519-85579087

Outcome results

None listed

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