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A Study on the Diagnostic and Therapeutic Efficacy of Long-Axis Spiral 3D Scanning in Interventional Treatment of Anterior and Posterior Communicating Arteries Aneurysms

A Study on the Diagnostic and Therapeutic Efficacy of Long-Axis Spiral 3D Scanning in Interventional Treatment of Anterior and Posterior Communicating Arteries Aneurysms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110024
Enrollment
Unknown
Registered
2025-09-29
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Anterior and posterior communicating artery aneurysm

Interventions

Panoramic 3D DSA group (self-intervention group):Panoramic 3D DSA
Traditional 3D DSA group (self-controlled group):Traditional 3D DSA Group

Sponsors

Henan Provincial People's Hospita,medical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years, with suspected intracranial aneurysm based on initial screening via CTA/MRA or similar imaging; 2.The patient signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Renal dysfunction; 2. Significant reduction in peripheral white blood cell or platelet count, or severe and uncorrectable coagulation disorder; 3. History of diagnosed cerebral vasculitis, brain tumor, or brain trauma within the past 3 months; 4. Active bleeding or recent hemorrhage within the last 30 days; 5. Severe head trauma within the past 3 months resulting in persistent neurological deficits; 6. Hypertension poorly controlled by medication; 7. Suspected aortic dissection; 8. Currently participating in another drug or medical device study; 9. Patients deemed unsuitable for participation by the investigator; 10. Severe diseases of vital organs such as heart, lung, or brain; 11. Allergy to iodinated contrast agents; 12. Pregnant or lactating women; 13. Inability to cooperate with examinations (e.g., impaired consciousness, severe agitation); 14. Severe disruption of the imaging procedure due to unforeseen factors; 15. Missing critical data; 16. Intracranial hemorrhage identified on imaging.

Design outcomes

Primary

MeasureTime frame
Subjective Scoring of Aneurysm Visualization;

Secondary

MeasureTime frame
Radiation dose received by the operator during carotid compression;

Countries

China

Contacts

Public ContactWang Meiyun

Henan Provincial People's Hospita,medical

mywang@zzu.edu.cn+86 371 87160596

Outcome results

None listed

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