Clinical Trials Directory

Trials / Unknown

UnknownNCT01922609

Prediction of Carotid Occlusion Intolerance by Transcranial Doppler Evaluation in Patients Undergoing Carotid Artery Stenting With Proximal Flow Arrest Protection System.

Status
Unknown
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
University Hospital, Motol · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

The aim of this observational pilot study is to determine whether intolerance of carotid occlusion during carotid artery stenting can be predicted with preprocedural transcranial Doppler evaluation.

Detailed description

Carotid artery stenting procedures are increasingly performed with devices that involve endovascular clamping of the common carotid artery, thus exposing the ipsilateral hemisphere to hypoperfusion. Approximately 5% of patients do not tolerate the clamp and are in increased risk of periprocedural cerebrovascular complication such as transient ischemic attack or stroke. To date, there is no method available that could be used to predict the risk of occlusion intolerance. The aim of this study is to determine whether preprocedural evaluation with transcranial Doppler ultrasonography can be effective in prediction of occlusion intolerance.

Conditions

Timeline

Start date
2013-05-01
Primary completion
2015-08-01
First posted
2013-08-14
Last updated
2013-08-14

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT01922609. Inclusion in this directory is not an endorsement.