Mechanical Thrombectomy Of Acute Occlusion In Ischemic Stroke

May 4, 2017 updated by: AHMohamed, Assiut University
Assessment of Therapeutic benefits and hazards of Mechanical Thrombectomy in Ischemic stroke patients with proximal occlusion within 4.5 hours from stroke onset.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Stroke is an acute neurologic dysfunction of vascular origin with sudden or at least rapid occurrence of symptoms and signs corresponding to the involvement of focal areas in the brain.The two main types of stroke are ischemic and hemorrhagic.Thrombosis can form in the extracranial and intracranial arteries when the intima is roughened and plaque forms along the injured vessel.The endothelial injury permits platelets to adhere and aggregate, then coagulation is activated and thrombus develops at site of plaque.Blood flow through the extracranial and intracranial systems decreases, and the collateral circulation maintains function. When the compensatory mechanism of collateral circulation fails, perfusion is compromised, leading to decreased perfusion and cell death. Stroke is the third leading cause of death in the United States. Many people die each year from stroke in the United States.Stroke is the leading cause of serious, long-term disability in the United States. Nearly one fourth of strokes occur in people under the age of 65.High blood pressure is the most important risk factor for stroke. Intravenous recombinant tissue-type plasminogen activator is the only Food and Drug Administration approved treatment for acute ischemic stroke. Mechanical thrombectomy improves clinical outcomes in patients with acute ischemic stroke caused by a large vessel occlusion.There is no apparent benefit of intravenous thrombolysis to patients with ischemic stroke undergoing mechanical thrombectomy. The study will be performed involving ischemic stroke patients with proximal occlusion within 4.5 hours from stroke onset.

Study Type

Interventional

Enrollment (Anticipated)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Aged between 18 - 80 years old of both sex.
  2. Acute ischemic stroke due to proved large-artery occlusion.
  3. Ineligibility for IV thrombolysis.
  4. A timeframe of ≤ 4.5 hours between stroke onset and the start of mechanical thrombectomy.
  5. The patients included in this series should have an NIHSS score of at least 10 or fluctuating symptoms.
  6. ASPECTS of 6 or > 6
  7. All patients will be undergoing CT/CT angiography before and after treatment

Exclusion Criteria:

  1. Age older than 80 years or less than 18
  2. Cerebral haemorrhage.
  3. Acute infarction > 1/3 of middle cerebral artery (MCA) territory on CT-scan.
  4. A history of stroke in the last 6 weeks.
  5. A time interval of > 4.5 hours.
  6. laboratory evidence of coagulation abnormalities.
  7. Known arteriovenous malformation , neoplasm or aneurysm.
  8. Woman at child bearing age who has a positive pregnancy test

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: mechanical thrombectomy
The study will be performed involving ischemic stroke patients with proximal occlusion within 4.5 hours from stroke onset, mechanical thrombectomy with retrievable stents, thrombus aspiration, retraction, wire disruption.
mechanical thrombectomy with retrievable stents, thrombus aspiration, retraction, wire disruption

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Treatment Of Acute Occlusion In Ischemic Stroke by Mechanical Thrombectomy
Time Frame: 18 months

Treatment of ischemic stroke patients after 4.5 hours from stroke onset by endovascular intervention by using Mechanical Thrombectomy techniques and without using Recombinant tissue-type plasminogen Activator and non eligible patients for Thrombectomy will be excluded.

The number of people will be participated into this study will be 20 aged 18 to 80 years old The patients will be undergoing NIHSS score , ASPECTS score The patients will be undergoing CT/CT angiography The patients will be undergoing mechanical thrombectomy Results will be collected and correlated with the prognosis of the outcomes

18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The patients will be undergoing NIHSS score
Time Frame: 1 hour
patients with NIHSS score less than 10 non eligible for mechanical thrombectomy
1 hour
The patients will be undergoing ASPECTS score
Time Frame: 1 hour
patients with ASPECTS score less than 6 non eligible for mechanical thrombectomy
1 hour
The patients will be undergoing CT/CT angiography
Time Frame: 2 hours
ct and ct angiography for exclusion of any bleeding or head injury
2 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

November 1, 2017

Primary Completion (Anticipated)

November 1, 2018

Study Completion (Anticipated)

December 1, 2019

Study Registration Dates

First Submitted

April 17, 2017

First Submitted That Met QC Criteria

May 4, 2017

First Posted (Actual)

May 9, 2017

Study Record Updates

Last Update Posted (Actual)

May 9, 2017

Last Update Submitted That Met QC Criteria

May 4, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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