Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01830413
Other study ID # stent-2013
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 10, 2013
Last updated April 18, 2013
Start date April 2013
Est. completion date December 2013

Study information

Verified date April 2013
Source Beijing Tiantan Hospital
Contact yilong Wang, M.D.
Phone 86-13911666571
Email yilong528@gmail.com
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational [Patient Registry]

Clinical Trial Summary

Stenting for systematic Intracranial artery stenosis is challenged recently, especially for safety. This registry is aimed to explore the safety profile during peri-operation period in Stenting procedures for systematic Intracranial artery stenosis in Chinese population in real world.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 450
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- 18-80 year old

- medical failure patient with systematic Intracranial artery stenosis

- More than 3 weeks after most recent ischemic stroke

- Digital Subtraction Angiography(DSA) showed =70% stenosis in target intracranial artery

- Imaging test within 1 week showed bad collateral circulation in target vessel area

- Diseased vessel diameter=2mm, length <15mm, distal vessel is normal

Exclusion Criteria:

- Diffused intracranial stenosis

- Acute stroke or TIA within 3 weeks

- Pure penetrating branch stenosis showed by cerebral imaging

- Non-atherosclerosis pathology for the stenosis

- Intracranial hemorrhage in target vessel area within 6 weeks; or potential cardiac thrombus source

- Intracranial tumor, arterial aneurysm or intracranial arteriovenous malformation

•>50% stenosis in extracranial carotid artery or vertebral artery in operation side; Known contradiction to heparin, aspirin, clopidogrel, anesthesia or contrast; hemoglobin <10g/dl,platelet count <100000

- Modified Rankin score =3 related to target vessel;

- INR(International Normalized Ratio)>1.5(irreversible),persist hemorrhage risk; life expectancy < 1year

- Pregnant or beast-feeding

- Not suitable for endovascular stenting judged by Indication Judgement Committee

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China Beijing Tiantan Hospital Beiing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Tiantan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety during peri-operation period Stroke in target cerebral vessel or death within 30 days after stenting procedure for systematic Intracranial artery stenosis 30 days after operation Yes
Secondary Recurrent stroke in 30days to 1 year after stenting in target vessel area. Recurrent stroke in 30days to 1 year after stenting in target vessel area. 30days to 1 year after stenting No
Secondary Successful recanalization rate right after stenting right after stenting No
Secondary Stent restenosis rate Within 1 year after stenting No
Secondary Ischemic stroke outside target vessel area 30 days - 1 year after stenting No
Secondary Cerebral haemorrhage 30 days - 1year after Yes
Secondary Myocardial infarction within 1 year Yes
Secondary non-stroke haemorrhage within 1year Yes
Secondary Death in 30 days- 1 year after stenting 30 days- 1 year after stenting Yes
Secondary disabled stroke within 1year Yes
Secondary Any stroke or death within 1 year Yes
Secondary Serious adverse event within 1year Yes
Secondary National Institutes of Health Stroke Scale score(NIHSS score) at 30 days and 1 year after stenting No
Secondary Modified Rankin score(mRS) at 30 days and 1 year after stenting No
Secondary MoCA scale score at 30 days and 1 year after stenting No
Secondary Life quality scale score at 1 year after stenting No