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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02846259
Other study ID # SKW2016-13-aspirin
Secondary ID
Status Recruiting
Phase N/A
First received July 25, 2016
Last updated November 9, 2016
Start date January 2016
Est. completion date December 2019

Study information

Verified date November 2016
Source Beijing Tiantan Hospital
Contact Yong Cao, M.D.
Phone 010-67096523
Email caoyong6@hotmail.com
Is FDA regulated No
Health authority China: Beijing Municipal Science and Technology Commission
Study type Observational [Patient Registry]

Clinical Trial Summary

The first purpose of this study is to find out the clinical benefit and risk of oral aspirin for unruptured intracranial aneurysm (small than 7mm) combined with cerebral ischemia in patients in the real world.

The second purpose of this study is to get the prediction model of aneurysm's rupture in patients who has unruptured intracranial aneurysm (small than 7mm) combined with cerebral ischemia , and find out who is suitable for oral aspirin.


Description:

The investigators try to collect the information of the patients have unruptured intracranial aneurysm combined with cerebral ischemia when oral aspirin.The characteristics of this study are large sample, multi center and prospective.In the real world, more and more patients are checked out unruptured intracranial aneurysm combined with cerebral ischemia.The investigators can collect the information such as how they use aspirin (dose, frequency, duration of treatment), demographic information, past history, daily life habits, morphological characteristics of the aneurysm, how they use other antithrombotic drugs.The investigators will record whether the aneurysm ruptured and have hemorrhage, ischemic stroke, death, changes in the morphology of aneurysm, MRI permeability image index changes. Finally the investigators will get the clinical benefits and risks of using aspirin and build the prediction model of rupture and hemorrhage for aneurysm, find out who is suitable for oral aspirin.


Recruitment information / eligibility

Status Recruiting
Enrollment 2135
Est. completion date December 2019
Est. primary completion date March 2019
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. has the diagnosis of unruptured intracranial aneurysm (using the CTA/DSA,smaller than 7mm)

2. has the history of TIA or any other diseases of cerebral ischemia

3. older than 18 years old

4. sign the informed consent

Exclusion Criteria:

1. has the history of intracranial aneurysm rupture hemorrhage or has more than one aneurysm untreated

2. has a family history of intracranial aneurysm

3. has AVM,MMD, intracranial tumor, hydrocephalus or intracranial hemorrhage

4. refuse to sign the informed consent

5. allergic to contrast medium

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
China Beijing Tiantan Hospital, Capital Medical University Beijing Beijing

Sponsors (7)

Lead Sponsor Collaborator
Beijing Tiantan Hospital Beijing Chao Yang Hospital, Beijing Friendship Hospital, The Second Hospital of Hebei Medical University, Tianjin Huanhu Hospital, Tianjin Medical University General Hospital, Xuanwu Hospital, Beijing

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Aneurysm rupture hemorrhage Aneurysm subarachnoid hemorrhage without trauma 2 years during the follow-up period No
Secondary TIA 2 years during the follow-up period No
Secondary Aneurysm changing the aneurysm becomes bigger, its form changes, becomes two or more 2 years during the follow-up period No
Secondary dead 2 years during the follow-up period No
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