- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03144960
Mechanical Thrombectomy Of Acute Occlusion In Ischemic Stroke
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged between 18 - 80 years old of both sex.
- Acute ischemic stroke due to proved large-artery occlusion.
- Ineligibility for IV thrombolysis.
- A timeframe of ≤ 4.5 hours between stroke onset and the start of mechanical thrombectomy.
- The patients included in this series should have an NIHSS score of at least 10 or fluctuating symptoms.
- ASPECTS of 6 or > 6
- All patients will be undergoing CT/CT angiography before and after treatment
Exclusion Criteria:
- Age older than 80 years or less than 18
- Cerebral haemorrhage.
- Acute infarction > 1/3 of middle cerebral artery (MCA) territory on CT-scan.
- A history of stroke in the last 6 weeks.
- A time interval of > 4.5 hours.
- laboratory evidence of coagulation abnormalities.
- Known arteriovenous malformation , neoplasm or aneurysm.
- Woman at child bearing age who has a positive pregnancy test
Study Plan
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
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Thrombectomy
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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