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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02354300
Other study ID # 201400923
Secondary ID
Status Completed
Phase N/A
First received January 29, 2015
Last updated August 25, 2016
Start date April 2015
Est. completion date May 2015

Study information

Verified date August 2016
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Flow diverters have been approved since 2012 for the treatment of large, wide neck intracranial aneurysms. These devices have been associated with embolic events which cause blockage in a blood vessel and can result in long term complications. One possible cause of these events is the formation of small emboli during placement of the device.


Description:

Flow diverters have been developed to treat intracranial aneurysms. Embolisms have occurred in a small percentage of patients which can result in long term complications including stroke, hemorrhage, and even death.

The formation of microemboli during the insertion of the device has not been evaluated. During insertion, there is significant disruption of blood flow and this may be a source of intracranial microemboli.

This study will use transcranial doppler ultrasound (TCD) to evaluate the blood flow during the placement of flow diverters to try to determine why these embolic events occur.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date May 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult subjects 18 years of age and older

- Non-pregnant

- Diagnosis of intracranial aneurysm that will be clinically treated with a flow diverter

Exclusion Criteria:

- Pregnant

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Device:
TCD Ultrasound
Transcranial doppler ultrasound monitoring will occur during flow diverter placement.

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Occurence of microemboli The number of subjects who experience microemboli during device placement. 1 day No
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