Skip to main content
Clinical Trials/NCT03153878
NCT03153878
Unknown
Not Applicable

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

Liu Zhiyong0 sites1,800 target enrollmentJune 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intracranial Aneurysm
Sponsor
Liu Zhiyong
Enrollment
1800
Primary Endpoint
Aneurysm rupture
Last Updated
8 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
June 1, 2017
End Date
December 31, 2021
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Liu Zhiyong
Responsible Party
Sponsor Investigator
Principal Investigator

Liu Zhiyong

Research associate

West China Hospital

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of untreated unruptured intracranial aneurysm (by CTA, MRA or DSA);
  • Patient with premorbid mRS of 3 or less;
  • Patient older than 14years;
  • Patient consenting to participate to the study;
  • 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 \[DRAFT\] -
  • Patient with other cerebral arteriovenous malformations or cerebral arteriovenous fistulas;
  • Patient with malignant tumor;
  • Target aneurysm is fusiform, traumatic, mycotic, or dissecting related;
  • Inability to obtain informed consent;
  • Patients with a life expectancy less than 1 year;
  • Participating in the other clinical studies of intracranial aneurysm;
  • Refusal of follow-up

Outcomes

Primary Outcomes

Aneurysm rupture

Time Frame: Up to 4 years or time of aneurysm repair surgery

Aneurysm rupture

Morphological changes of aneurysms

Time Frame: Up to 4 years or time of aneurysm repair surgery

maximum diameter increase ≥ 1mm or appearance of a daughter sac

Secondary Outcomes

  • Acute myocardial infarction(Up to 4 years])
  • New onset ischemic stroke(Up to 4 years])

Similar Trials