About this trial
If the participants agree to participate in this study, the participants will undergo two scans (classic 3D-DSA and PS-3D-DSA assisted scan) to compare the imaging effects of both. After the procedure, the investigators will record the radiation exposure and collect DSA images.
Eligibility criteria
Qualifiers
Age ≥18 years.
Requires 3D-DSA-guided interventional diagnosis or treatment (e.g., cerebral angiography, cerebral artery chemoembolization) and meets operational indications.
Can understand the study's purpose, procedures, potential risks, and benefits, and voluntarily signs a written informed consent form.
Disqualifiers
Severe heart or lung disease, such as heart failure or chronic obstructive pulmonary disease (COPD).
History of high-dose radiation exams or treatments.
Known allergies or severe adverse reactions to iodine contrast agents or other relevant medications.
Pregnant or breastfeeding women.
Trial design
Treatments tested in this trial
- PS-3D-DSA
- classic 3D-DSA
Treatment groups
Sponsors and collaborators
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead sponsor
Huazhong University of Science and Technology
Sponsor institution