Clinical Trials Directory

Trials / Completed

CompletedNCT01632865

Recanalization and Stenting for Non-acute Veterbrobasilar Artery Occlusion

Recanalization and Stenting for Subacute and Chronic Veterbrobasilar Artery Occlusion

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Zhengzhou University · Academic / Other
Sex
All
Age
30 Years
Healthy volunteers
Not accepted

Summary

To evaluate whether recanalization and stenting for symptomatic subacute and chronic veterbrobasilar artery occlusion is technically feasible, can prevent from recurrent ischemic events and promotes functional recovery of disability.

Detailed description

Ischemic stroke accounts for 87% of cerebrovascular accidents. Of these, a part is the result of intracranial veterbrobasilar occlusion. Acute veterbrobasilar artery occlusion is a devastating disease with high mortality without successful treatment. A subset of patients can survive the acute phase and develop subacute or chronic veterbrobasilar artery occlusion. Due to the adequacy of collaterals, some patients can live without any or just very mild symptoms. On the contrast, lack of enough collaterals, another patients still presented with recurrent ischemic events and progressive disability despite intensive medical therapy. Prognosis is extremely poor. It is in this cohort that subacute or chronic revascularization is often considered. The optimal treatment in this cohort with non-acute veterbrobasilar artery occlusion is unknown, and there is little literature to guide therapy. Extracranial-intracranial bypass may revascularize the intracranial artery occlusion. However, bypass procedures are technically challenging and are associated with significant risk of morbidity and mortality. Recurrent ischemic symptoms despite best medical treatment be indication for endovascular revascularization and stent remodeling. This study was to evaluate the technical feasibility, safety and treatment effects of recanalization and stenting for veterbrobasilar subacute-chronic intracranial artery occlusion。

Conditions

Interventions

TypeNameDescription
DEVICEstentingApollo stent (MicroPort Medical, China),Neuroform stent (Stryker/Boston Scientific, USA) or Wingspan stent (Stryker/Boston Scientific, USA), et al.

Timeline

Start date
2013-04-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2012-07-03
Last updated
2017-01-25

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT01632865. Inclusion in this directory is not an endorsement.