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The Capillary Index Score Trial

Primary Purpose

Acute Stroke, Brain Ischemia, Ischemic Stroke

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Endovascular Treatment (EVT)
Sponsored by
Firas Al-Ali
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Acute Stroke focused on measuring capillary index score, acute ischemic stroke, collateral circulation, cerebral ischemia, diagnostic imaging

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Anterior circulation acute ischemic stroke due to blockage of the intracranial internal carotid artery or middle cerebral artery (M1)
  2. Within 24 hours of onset of symptoms
  3. NIHSS Score is 8 or greater

Exclusion Criteria:

  1. Contra-indication for IAT found on initial CT
  2. Intracranial hemorrhage
  3. Stroke mimics (tumor, herpetic encephalitis, etc.)
  4. More than 1/3 hypodensity on non-enhanced head CT prior to intervention
  5. ASPECT Score less than 6
  6. Pre-existing disability defined as modified Rankin Scale (mRS) score more than 2
  7. Pregnant women

Sites / Locations

  • WellStar Atlanta Medical System
  • New York University Langone Medical Center
  • Rochester General Hospital
  • University of North Carolina Hospital
  • Akron General Medical Center
  • University of Vermont Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Favorable CIS

Poor CIS

Arm Description

Patients with a favorable CIS (fCIS) will receive endovascular treatment (EVT) and medical treatment consistent with national guidelines.

Patients with a poor CIS (pCIS) will receive endovascular treatment (EVT) and medical treatment consistent with national guidelines.

Outcomes

Primary Outcome Measures

Modified Rankin Score (mRS) Between Favorable CIS Group Versus Poor CIS Group.
The mRS Score ranges from 0-6 and describes the degree of disability or dependence after a stroke. The grades are no symptoms (0), no significant disability (1), slight disability (2), moderate disability (3), moderately severe disability (4), severe disability (5), and death (6).

Secondary Outcome Measures

Complication Rate Between Favorable CIS Group Versus Poor CIS Group
Complication : Clinically relevant intracranial hemorrhage and vasogenic edema as defined by parenchymal hematoma (PH) 1 or 2
Modified Rankin Score (mRS) Between Favorable CIS With Good Revascularization Versus Poor CIS With Good Revascularization.
Revascularization status will be classified as poor (mTICI = 0-2A) or good (mTICI = 2B, 3). Rate of good clinical outcomes between groups will be compared based on the combination of CIS and revascularization status. Good outcome will be measured based on the modified Rankin scale score according to: 0: No symptoms No significant disability despite symptoms Slight disability Moderate disability Moderately severe disability Severe disability Dead A score of 0-2 is considered a good outcome

Full Information

First Posted
November 26, 2015
Last Updated
January 23, 2020
Sponsor
Firas Al-Ali
Collaborators
Stryker Neurovascular, Rochester General Hospital, University of Vermont Medical Center, University of North Carolina, Chapel Hill, NYU Langone Health, WellStar Health System
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1. Study Identification

Unique Protocol Identification Number
NCT02618031
Brief Title
The Capillary Index Score Trial
Official Title
The Capillary Index Score Trial: Phase I
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
March 1, 2016 (Actual)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Firas Al-Ali
Collaborators
Stryker Neurovascular, Rochester General Hospital, University of Vermont Medical Center, University of North Carolina, Chapel Hill, NYU Langone Health, WellStar Health System

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study seeks to investigate the capillary index score (CIS) to further improve patient selection of endovascular treatment (EVT) in acute ischemic stroke (AIS). The hypothesis or idea being tested: Patients with favorable CIS who are successfully revascularized with EVT can have successful outcomes with an extended time window for treatment.
Detailed Description
This study is trying to look at how the well-being of the patient following treatment is influenced by peripheral blood supply (collateral flow) to the area lacking primary blood flow due to the clot. Treatment of AIS includes EVT and medical treatment. EVT is typically not offered to patients after 6 hours of the onset of symptoms. The current study is based on the belief that patients can be successfully treated with the EVT up to 8 hours, as long as they have good peripheral blood flow (collateral flow) to the area of tissue blocked of the primary blood supply. The study will evaluate the ability of the capillar index score (CIS) to identify patients who can be successfully treated with EVT. The CIS quantifies blood supply to the ischemic area from peripheral vessels (collateral flow) based on diagnostic cerebral angiogram. Patients are graded on a scale from 0-3, with 0 and 1 considered a poor CIS (pCIS) and 2 and 3 considered a favorable CIS (fCIS). All patients will be treated with EVT and medical treatment consistent with national guidelines. The primary endpoint is the clinical outcome at 90 days between fCIS group versus pCIS group. The secondary endpoint is the influence of successful revascularization on outcomes for patients with fCIS or pCIS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Stroke, Brain Ischemia, Ischemic Stroke
Keywords
capillary index score, acute ischemic stroke, collateral circulation, cerebral ischemia, diagnostic imaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Patients will be assigned to one of two groups based on the outcome of diagnostic evaluation. Treatment will be identical for the two groups.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The participants and investigators evaluating 90 day outcomes will be blinded to the group.
Allocation
Non-Randomized
Enrollment
57 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Favorable CIS
Arm Type
Other
Arm Description
Patients with a favorable CIS (fCIS) will receive endovascular treatment (EVT) and medical treatment consistent with national guidelines.
Arm Title
Poor CIS
Arm Type
Experimental
Arm Description
Patients with a poor CIS (pCIS) will receive endovascular treatment (EVT) and medical treatment consistent with national guidelines.
Intervention Type
Procedure
Intervention Name(s)
Endovascular Treatment (EVT)
Other Intervention Name(s)
Intra-arterial Treatment (IAT)
Intervention Description
EVT is an endovascular procedure in which a catheter is inserted into an artery and directed to the site of the blocked blood vessel in the brain. The clot is removed using a mechanical device with or without an injection of tPA (tissue plasminogen activator) directly at the site of the clot. The protocol calls for use of the Trevo stent retriever (Stryker Neurovascular) for the first pass of clot removal.
Primary Outcome Measure Information:
Title
Modified Rankin Score (mRS) Between Favorable CIS Group Versus Poor CIS Group.
Description
The mRS Score ranges from 0-6 and describes the degree of disability or dependence after a stroke. The grades are no symptoms (0), no significant disability (1), slight disability (2), moderate disability (3), moderately severe disability (4), severe disability (5), and death (6).
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Complication Rate Between Favorable CIS Group Versus Poor CIS Group
Description
Complication : Clinically relevant intracranial hemorrhage and vasogenic edema as defined by parenchymal hematoma (PH) 1 or 2
Time Frame
1 day - 1 week
Title
Modified Rankin Score (mRS) Between Favorable CIS With Good Revascularization Versus Poor CIS With Good Revascularization.
Description
Revascularization status will be classified as poor (mTICI = 0-2A) or good (mTICI = 2B, 3). Rate of good clinical outcomes between groups will be compared based on the combination of CIS and revascularization status. Good outcome will be measured based on the modified Rankin scale score according to: 0: No symptoms No significant disability despite symptoms Slight disability Moderate disability Moderately severe disability Severe disability Dead A score of 0-2 is considered a good outcome
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Anterior circulation acute ischemic stroke due to blockage of the intracranial internal carotid artery or middle cerebral artery (M1) Within 24 hours of onset of symptoms NIHSS Score is 8 or greater Exclusion Criteria: Contra-indication for IAT found on initial CT Intracranial hemorrhage Stroke mimics (tumor, herpetic encephalitis, etc.) More than 1/3 hypodensity on non-enhanced head CT prior to intervention ASPECT Score less than 6 Pre-existing disability defined as modified Rankin Scale (mRS) score more than 2 Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Firas Al-Ali, MD
Organizational Affiliation
Cleveland Clinic Akron General
Official's Role
Principal Investigator
Facility Information:
Facility Name
WellStar Atlanta Medical System
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30312
Country
United States
Facility Name
New York University Langone Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Rochester General Hospital
City
Rochester
State/Province
New York
ZIP/Postal Code
14621
Country
United States
Facility Name
University of North Carolina Hospital
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27514
Country
United States
Facility Name
Akron General Medical Center
City
Akron
State/Province
Ohio
ZIP/Postal Code
44307
Country
United States
Facility Name
University of Vermont Medical Center
City
Burlington
State/Province
Vermont
ZIP/Postal Code
05401
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25954243
Citation
Al-Ali F, Elias JJ, Filipkowski DE, Faber JE. Acute ischemic stroke treatment, part 1: patient selection "the 50% barrier and the capillary index score". Front Neurol. 2015 Apr 22;6:83. doi: 10.3389/fneur.2015.00083. eCollection 2015.
Results Reference
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PubMed Identifier
26082751
Citation
Al-Ali F, Elias JJ, Filipkowski DE. Acute Ischemic Stroke Treatment, Part 2: Treatment "Roles of Capillary Index Score, Revascularization and Time". Front Neurol. 2015 Jun 1;6:117. doi: 10.3389/fneur.2015.00117. eCollection 2015.
Results Reference
background
PubMed Identifier
25953374
Citation
Al-Ali F, Elias JJ, Tomsick TA, Liebeskind DS, Broderick JP; IMS Study Groups. Relative Influence of Capillary Index Score, Revascularization, and Time on Stroke Outcomes From the Interventional Management of Stroke III Trial. Stroke. 2015 Jun;46(6):1590-4. doi: 10.1161/STROKEAHA.115.009066. Epub 2015 May 7.
Results Reference
background
PubMed Identifier
24851874
Citation
Al-Ali F, Tomsick TA, Connors JJ 3rd, Gebel JM, Elias JJ, Markarian GZ, Al-Ali Z, Broderick JP. Capillary Index Score in the Interventional Management of Stroke trials I and II. Stroke. 2014 Jul;45(7):1999-2003. doi: 10.1161/STROKEAHA.114.005304. Epub 2014 May 22.
Results Reference
background
PubMed Identifier
22266703
Citation
Al-Ali F, Jefferson A, Barrow T, Cree T, Louis S, Luke K, Major K, Nemeth D, Smoker S, Walker S. The capillary index score: rethinking the acute ischemic stroke treatment algorithm. Results from the Borgess Medical Center Acute Ischemic Stroke Registry. J Neurointerv Surg. 2013 Mar;5(2):139-43. doi: 10.1136/neurintsurg-2011-010146. Epub 2012 Jan 19.
Results Reference
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The Capillary Index Score Trial

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