Skip to content

The Prospective Cohort Study on the Benefit-risk of Antithrombotic or Anticoagulant Therapy in Patients With Unruptured Intracranial Aneurysms Associated With Ischemic Heart Disease or Ischemic Cerebrovascular Disease

The Prospective Cohort Study on the Benefit-risk of Antithrombotic or Anticoagulant Therapy in Patients With Unruptured Intracranial Aneurysms Associated With Ischemic Heart Disease or Ischemic Cerebrovascular Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03153878
Enrollment
1800
Registered
2017-05-15
Start date
2017-06-01
Completion date
2021-12-31
Last updated
2017-05-15

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

Conditions

Intracranial Aneurysm, Ischemic Cerebrovascular Disease, Ischemic Heart Disease, Natural History

Keywords

Unruptured Intracranial Aneurysm, Benefit-risk, Ischemic heart disease, Ischemic cerebrovascular disease, Antithrombotic, Anticoagulant, People's Republic of China, Multicenter Studies

Brief summary

This is a registry study of the natural course of unruptured intracranial aneurysms (UIA). In addition, the investigators will analyze the benefit-risk of antithrombotic or anticoagulant therapy in patients with unruptured intracranial aneurysms associated with ischemic heart disease or ischemic cerebrovascular disease. The investigators aim to use research data to create a China national database of UIA

Detailed description

This is a registry study of the natural course of unruptured intracranial aneurysms (UIA). In addition, the investigators will analyze the benefit-risk of antithrombotic or anticoagulant therapy in patients with unruptured intracranial aneurysms associated with ischemic heart disease or ischemic cerebrovascular disease. The investigators aim to use research data to create a China national database of UIA. This study is supported by a research grant from the Ministry of Science and Technology of the People's Republic of China. The investigators will collaborate with the other 19 medical centers which locate in the different districts of China. During the study period, all the patients included in this study will observe and treat in the collaborating medical centers. Included patients will be followed-up for at least 1year. Research data will represent the real natural course of UIA in China. For this study, the investigators consulted and hired professional experts about data collection, data and methodology. An intact systematic project steering committee, including Data Monitoring Committee, Data Management Committee, Project Academic Committee, Executive Group, Project Manager, Project Statistician, and Technical Support Center has been built up. Scientific regulations have also been made

Interventions

None listed

Sponsors

Xuanwu Hospital, Beijing
CollaboratorOTHER
Liu Zhiyong
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
14 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of untreated unruptured intracranial aneurysm (by CTA, MRA or DSA); 2. Patient with premorbid mRS of 3 or less; 3. Patient older than 14years; 4. Patient consenting to participate to the study; 5. Patients with a definite history of ischemic heart disease or ischemic stroke who accept antithrombotic or anticoagulant therapy for secondary pevention

Exclusion criteria

Subarachnoid hemorrhage with unknown causes; \- Page 4 of 4 \[DRAFT\] - 2. Patient with other cerebral arteriovenous malformations or cerebral arteriovenous fistulas; 3. Patient with malignant tumor; 4. Target aneurysm is fusiform, traumatic, mycotic, or dissecting related; 5. Inability to obtain informed consent; 6. Patients with a life expectancy less than 1 year; 7. Participating in the other clinical studies of intracranial aneurysm; 8. Refusal of follow-up

Design outcomes

Primary

MeasureTime frameDescription
Aneurysm ruptureUp to 4 years or time of aneurysm repair surgeryAneurysm rupture
Morphological changes of aneurysmsUp to 4 years or time of aneurysm repair surgerymaximum diameter increase ≥ 1mm or appearance of a daughter sac

Secondary

MeasureTime frameDescription
Acute myocardial infarctionUp to 4 years]Acute myocardial infarction
New onset ischemic strokeUp to 4 years]New onset ischemic stroke

Contacts

Primary ContactZhiyong Liu, M.D, Ph.D
doctor_lzy@163.com+8613658021726
Backup ContactJin Li, M.D, Ph.D
jimlijin76@126.com+13683482059

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026