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Clinical Trials in China / NCT06902415
Recruiting Observational

Application of QDSA Platform in Cerebrovascular Diseases

NCT06902415 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Tiantan Hospital
Phase
Observational
Started
2025-04
Last updated
2025-03-30

Condition(s) studied

Cerebrovascular Disease

Investigational drug(s) / intervention(s)

QDSA (Quantitative Digital Subtraction Angiography)

QDSA (Quantitative Digital Subtraction Angiography): QDSA is a quantitative analysis technology based on DSA, used to assess hemodynamic characteristics and provide critical data support for the diagnosis and treatment of cerebrovascular diseases.

Study summary

Cerebrovascular diseases pose a major global public health challenge, characterized by exceptionally high mortality and disability rates, with their pathogenesis closely linked to hemodynamic abnormalities. The quantitative digital subtraction angiography (QDSA) analysis platform, leveraging its advantages of vessel modeling-free operation, high computational efficiency, and DSA-equivalent sensitivity, has emerged as a novel hemodynamic assessment method with significant clinical potential. This study aims to establish a cerebrovascular disease cohort incorporating QDSA parameters to systematically validate the clinical value of this technology in preoperative evaluation and surgical planning, thereby providing evidence-based insights for optimizing diagnostic and therapeutic strategies.

Eligibility

Sex
ALL
Min age
1 Year
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Cerebrovascular diseases diagnosed and assessed by DSA for related risks and treatment options. 2. The DSA acquisition protocol complies with the standard procedure. 3. DSA images must include complete anteroposterior and lateral views. 4. Raw data must be available in DICOM format. 5. Image quality and pixel resolution must support data analysis. 6. Patients must undergo regular follow-ups. Exclusion Criteria: 1. Cerebrovascular diseases not diagnosed or risk-assessed using DSA. 2. Patients with DSA image quality insufficient for image analysis and processing. 3. Severe organ diseases with an expected survival period of less than 2 years. 4. Inability to cooperate with treatment and follow-up. 5. Participation in other clinical trials within the past 6 months. 6. Other conditions deemed by the investigator as unsuitable for participation in this trial.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing Tiantan Hospital Beijing Beijing Municipality Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06902415 on ClinicalTrials.gov ↗ ← All trials in China