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The Intra-arterial Vasospasm Trial (iVAST)

Primary Purpose

Cerebral Vasospasm

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Nicardipine
Verapamil
Nicardipine + Verapamil + Nitroglycerin
Sponsored by
Peng Roc Chen, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Cerebral Vasospasm focused on measuring cerebral vasospasm, aneurysmal subarachnoid hemorrhage, intra arterial drug treatment for cerebral vasospasm, nicardipine milrinone nitroglycerin verapamil

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patient, age 18-80 years old, with ruptured aneurysm(s) who experience cerebral vasospasm post operatively within 3-21 days.
  • Symptomatic vasospasm (clinical or TCD)
  • For centers that perform a routine day 7 angiogram post-aneurysm treatment - 50% or more stenosis seen on diagnostic angiogram for asymptomatic patients.

Exclusion Criteria:

  • Inability to obtain consent from patient or patients kin
  • Pregnant women
  • less than 18 years of age of more than 80 years of age
  • Hunt Hess Grade 5 SAH
  • Intra-arterial drug treatment in all 3 arterial territories

Sites / Locations

  • Yale School of Medicine
  • University of Illinois College of Medicine at Chicago
  • University of Michigan
  • Northwell HealthRecruiting
  • Lenox Hill
  • Wake Forest University Health Sciences
  • Geisinger ClinicRecruiting
  • Thomas Jefferson University
  • Temple University
  • University of Texas Medical School at HoustonRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Nicardipine

Verapamil

Nicardipine + Verapamil + Nitroglycerin

Arm Description

Group 1 : Nicardipine 5mg per circulation intra-arterial injection, Pharmacological angioplasty

Group 3: Verapamil 10mg per circulation intra-arterial injection, Pharmacological angioplasty

Group 4 : Nicardipine 5mg + Verapamil 10mg + Nitroglycerin 200mcg in 4cc 5 % dextrose in water , intra-arterial injection, Pharmacological angioplasty

Outcomes

Primary Outcome Measures

Post infusion improvement ratio(PIIR)
Post infusion improvement ratio(PIIR) = (B - A) / A A = pre-infusion blood vessel diameter B = post infusion blood vessel diameter PIIR across all four treatment arms will be compared and tested for statistical significance.

Secondary Outcome Measures

To grade clinical outcome using Modified Rankin score
Clinical outcome at 3 months post discharge from hospital after treatment will be evaluated using Modified Rankin score

Full Information

First Posted
November 12, 2013
Last Updated
May 10, 2023
Sponsor
Peng Roc Chen, MD
Collaborators
Yale University, Thomas Jefferson University, University of Illinois at Chicago, Wake Forest University Health Sciences, Temple University, Geisinger Clinic, Northwell Health, University of Michigan, Lenox Hill Hospital, Weatherhead Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01996436
Brief Title
The Intra-arterial Vasospasm Trial
Acronym
iVAST
Official Title
The Intra-arterial Vasospasm Trial(iVAST)- A Multi-center Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 29, 2016 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Peng Roc Chen, MD
Collaborators
Yale University, Thomas Jefferson University, University of Illinois at Chicago, Wake Forest University Health Sciences, Temple University, Geisinger Clinic, Northwell Health, University of Michigan, Lenox Hill Hospital, Weatherhead Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of the study is to determine the optimal intra-arterial drug treatment regimen for arterial lumen restoration post cerebral vasospasm following aneurysmal subarachnoid hemorrhage. The secondary objective is to evaluate clinical outcome at 90 days post discharge following optimal intra-arterial drug treatment for cerebral vasospasm. We hypothesize that Intra-arterial (IA) infusion of a combination of multiple vasodilators is more efficacious than single agent treatment cerebral vasospasm therapy. All procedures done as a part of this study are standard hospital care procedures done to treat cerebral vasospasm and all drugs to be used are FDA approved.
Detailed Description
The primary objective of the study is to determine the optimal intra-arterial drug treatment regimen for arterial lumen restoration post cerebral vasospasm following aneurysmal subarachnoid hemorrhage. The secondary objective is to evaluate clinical outcome at 90 days post discharge following optimal intra-arterial drug treatment for cerebral vasospasm. This study is a prospective multicenter randomized trial. The primary outcome measure is the Post infusion improvement ratio (PIIR) assessed 10 minutes after completion of the intra-arterial infusion. PIIR is a measure of arterial lumen diameter pre and post intra-arterial drug infusion in the presenting vasospasmic blood vessel. Modified Rankin score (mRS) at 3 months post hospital discharge will be recorded as a secondary outcome to assess clinical outcome. The interventions in this study are a part of routine standard of care (SOC) procedures for cerebral vasospasm treatment. Following surgical or endovascular intervention for aneurysmal Subarachnoid Hemorrhage (aSAH) if patients develop cerebral vasospasm refractory to maximal medical management, endovascular treatment by intra-arterial drug infusion of single drug agent or cocktail drug agents will be initiated. Study participants will be randomly assigned to one of the three treatment groups where one single drug agent or cocktail drug agents will be intra-arterially administered. Pre & post infusion vasospasmic vessel diameters will be compared. The change in diameter will be quantified based on the mean percentage change. Three months post hospital discharge, study participants will be followed up in clinic to evaluate clinical outcome. The study will require 330 patients in total. The patient population will be hospitalized patients presenting with cerebral vasospasm post aneurysmal subarachnoid hemorrhage. Subjects will be stratified by randomization into 3 treatment groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Vasospasm
Keywords
cerebral vasospasm, aneurysmal subarachnoid hemorrhage, intra arterial drug treatment for cerebral vasospasm, nicardipine milrinone nitroglycerin verapamil

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
330 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nicardipine
Arm Type
Active Comparator
Arm Description
Group 1 : Nicardipine 5mg per circulation intra-arterial injection, Pharmacological angioplasty
Arm Title
Verapamil
Arm Type
Active Comparator
Arm Description
Group 3: Verapamil 10mg per circulation intra-arterial injection, Pharmacological angioplasty
Arm Title
Nicardipine + Verapamil + Nitroglycerin
Arm Type
Active Comparator
Arm Description
Group 4 : Nicardipine 5mg + Verapamil 10mg + Nitroglycerin 200mcg in 4cc 5 % dextrose in water , intra-arterial injection, Pharmacological angioplasty
Intervention Type
Drug
Intervention Name(s)
Nicardipine
Other Intervention Name(s)
Cardene
Intervention Description
Pharmacological angioplasty: intra-arterial drug infusion via catheter to treat cerebral vasospasm
Intervention Type
Drug
Intervention Name(s)
Verapamil
Intervention Description
Pharmacological angioplasty: intra-arterial drug infusion via catheter to treat cerebral vasospasm
Intervention Type
Drug
Intervention Name(s)
Nicardipine + Verapamil + Nitroglycerin
Intervention Description
Pharmacological angioplasty: intra-arterial drug infusion via catheter to treat cerebral vasospasm
Primary Outcome Measure Information:
Title
Post infusion improvement ratio(PIIR)
Description
Post infusion improvement ratio(PIIR) = (B - A) / A A = pre-infusion blood vessel diameter B = post infusion blood vessel diameter PIIR across all four treatment arms will be compared and tested for statistical significance.
Time Frame
pre pharmacological angioplasty blood vessel diameter - 0 min, post pharmacological angioplasty blood vessel diameter- 10 min after infusion
Secondary Outcome Measure Information:
Title
To grade clinical outcome using Modified Rankin score
Description
Clinical outcome at 3 months post discharge from hospital after treatment will be evaluated using Modified Rankin score
Time Frame
3 months post discharge from hospital
Other Pre-specified Outcome Measures:
Title
Intra-cranial pressure
Description
Intra-cranial pressure will be measured 1 day prior to vasospasm treatment and 1 day after vasospasm treatment
Time Frame
1 day prior to procedure & 1 day after the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patient, age 18-80 years old, with ruptured aneurysm(s) who experience cerebral vasospasm post operatively within 3-21 days. Symptomatic vasospasm (clinical or TCD) For centers that perform a routine day 7 angiogram post-aneurysm treatment - 50% or more stenosis seen on diagnostic angiogram for asymptomatic patients. Exclusion Criteria: Inability to obtain consent from patient or patients kin Pregnant women less than 18 years of age of more than 80 years of age Hunt Hess Grade 5 SAH Intra-arterial drug treatment in all 3 arterial territories
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peng R Chen, MD
Phone
713-486-8016
Email
Peng.R.Chen@uth.tmc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Eddie Aguilar, BA
Phone
713-486-7764
Email
Eddie.Aguilar@uth.tmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peng R Chen, MD
Organizational Affiliation
University of Texas Medical School at Houston
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ketan R Bulsara, MD, MBA
Organizational Affiliation
UConn Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale School of Medicine
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520
Country
United States
Individual Site Status
Terminated
Facility Name
University of Illinois College of Medicine at Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Individual Site Status
Withdrawn
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Individual Site Status
Withdrawn
Facility Name
Northwell Health
City
Manhasset
State/Province
New York
ZIP/Postal Code
11030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Ledoux, MD
Phone
516-562-3590
First Name & Middle Initial & Last Name & Degree
Sarah Nazir
Email
snazir1@northwell.edu
Facility Name
Lenox Hill
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Individual Site Status
Withdrawn
Facility Name
Wake Forest University Health Sciences
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Individual Site Status
Terminated
Facility Name
Geisinger Clinic
City
Danville
State/Province
Pennsylvania
ZIP/Postal Code
17822
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clemens Schirmer, MD
First Name & Middle Initial & Last Name & Degree
Chelsea Derr
Email
cmderr1@geisinger.edu
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Individual Site Status
Withdrawn
Facility Name
Temple University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19140
Country
United States
Individual Site Status
Withdrawn
Facility Name
University of Texas Medical School at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sunil Sheth, MD
Email
Sunil.A.Sheth@uth.tmc.edu
First Name & Middle Initial & Last Name & Degree
Eddie Aguilar, BA
Phone
713-486-7764
Email
Eddie.Aguilar@uth.tmc.edu
First Name & Middle Initial & Last Name & Degree
Sunil Sheth, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18638721
Citation
Dorsch NW, King MT. A review of cerebral vasospasm in aneurysmal subarachnoid haemorrhage Part I: Incidence and effects. J Clin Neurosci. 1994 Jan;1(1):19-26. doi: 10.1016/0967-5868(94)90005-1.
Results Reference
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PubMed Identifier
12744357
Citation
Treggiari MM, Walder B, Suter PM, Romand JA. Systematic review of the prevention of delayed ischemic neurological deficits with hypertension, hypervolemia, and hemodilution therapy following subarachnoid hemorrhage. J Neurosurg. 2003 May;98(5):978-84. doi: 10.3171/jns.2003.98.5.0978. Erratum In: J Neurosurg. 2003 Dec;99(6):1119.
Results Reference
background
PubMed Identifier
3176090
Citation
Biller J, Godersky JC, Adams HP Jr. Management of aneurysmal subarachnoid hemorrhage. Stroke. 1988 Oct;19(10):1300-5. doi: 10.1161/01.str.19.10.1300. No abstract available.
Results Reference
background
PubMed Identifier
3895589
Citation
Kassell NF, Sasaki T, Colohan AR, Nazar G. Cerebral vasospasm following aneurysmal subarachnoid hemorrhage. Stroke. 1985 Jul-Aug;16(4):562-72. doi: 10.1161/01.str.16.4.562.
Results Reference
background
PubMed Identifier
18312091
Citation
Keuskamp J, Murali R, Chao KH. High-dose intraarterial verapamil in the treatment of cerebral vasospasm after aneurysmal subarachnoid hemorrhage. J Neurosurg. 2008 Mar;108(3):458-63. doi: 10.3171/JNS/2008/108/3/0458.
Results Reference
background
PubMed Identifier
19057319
Citation
Linfante I, Delgado-Mederos R, Andreone V, Gounis M, Hendricks L, Wakhloo AK. Angiographic and hemodynamic effect of high concentration of intra-arterial nicardipine in cerebral vasospasm. Neurosurgery. 2008 Dec;63(6):1080-6; discussion 1086-7. doi: 10.1227/01.NEU.0000327698.66596.35.
Results Reference
background
PubMed Identifier
15140728
Citation
Badjatia N, Topcuoglu MA, Pryor JC, Rabinov JD, Ogilvy CS, Carter BS, Rordorf GA. Preliminary experience with intra-arterial nicardipine as a treatment for cerebral vasospasm. AJNR Am J Neuroradiol. 2004 May;25(5):819-26.
Results Reference
background
PubMed Identifier
20098322
Citation
Pierot L, Aggour M, Moret J. Vasospasm after aneurysmal subarachnoid hemorrhage: recent advances in endovascular management. Curr Opin Crit Care. 2010 Apr;16(2):110-6. doi: 10.1097/MCC.0b013e3283372ef2.
Results Reference
background
PubMed Identifier
18239182
Citation
Fraticelli AT, Cholley BP, Losser MR, Saint Maurice JP, Payen D. Milrinone for the treatment of cerebral vasospasm after aneurysmal subarachnoid hemorrhage. Stroke. 2008 Mar;39(3):893-8. doi: 10.1161/STROKEAHA.107.492447. Epub 2008 Jan 31.
Results Reference
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The Intra-arterial Vasospasm Trial

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