Intracranial aneurysm
Conditions
Interventions
Experimental group (software group) :Firstly, upload the patients preoperative 3D-DSA imaging data to AneuGuide software to complete vascular 3D reconstruction, parameter extraction, and recommend the
Control group (traditional group):Completely relying on traditional experience decision-making to complete stent implantation.
Sponsors
The First Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Patients with aneurysms who plan to receive dense mesh stent implantation treatment; 2. 18 years old and above, regardless of gender; 3. Can provide complete preoperative and postoperative clinical and imaging data, and sign informed consent forms.
Exclusion criteria
Exclusion criteria: 1. The target aneurysm is spindle shaped, traumatic, fungal, vesicular, pseudoaneurysm, dissection aneurysm, or patients with arteriovenous malformation, arteriovenous fistula, or smoky disease related aneurysms; 2. Patients with incomplete or poor image quality that cannot be processed using software; 3. Patients who are unable to complete the expected follow-up; 4. Patients who cannot collect complete clinical information; 5. Patients with other serious diseases, such as malignant tumors, severe liver and kidney dysfunction, etc; 6. Pregnant or lactating patients; 7. Expected survival period<12 months; 8. Other situations deemed unsuitable for participation in the clinical trial after evaluation by the researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occlusion of arterial aneurysm; | — |
Secondary
| Measure | Time frame |
|---|---|
| Occlusion of arterial aneurysm;Proximal Stent Anchoring Site;Metal Coverage Ratio at Aneurysm Neck;Stent Foreshortening Length;Long-Term Complications;Short-Term Complications; | — |
Countries
China
Contacts
Public ContactFeng Fan
The First Affiliated Hospital of Zhengzhou University
Outcome results
None listed