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Safety Study of Post Intravenous tPA Monitoring in Ischemic Stroke (OPTIMIST)

Primary Purpose

Stroke, Ischemic Stroke

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
"Hopkins" post tPA for ischemic stroke monitoring protocol
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Stroke focused on measuring IV tPA, Thrombolysis, Stroke, Ischemic, Monitoring

Eligibility Criteria

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

Inclusion Criteria:

  • Ability to provide written informed consent (or a Legally Authorized Representative (LAR) available to provide informed consent) and comply with study assessments for the full duration of the study.
  • Age 18-80 years
  • Patients to be included will be diagnosed as having an acute ischemic stroke by history and physical exam and receive IV tPA within 4.5 hours of symptom onset according to current guidelines for acute stroke care.
  • NIHSS at presentation <10
  • Patients do not have ICU needs in the judgment of the treating ED physician or neurologist by the end of the tPA infusion
  • NIHSS at the end of tPA infusion <10

Exclusion Criteria:

  • For patients receiving IV tPA according to the current standard of care, the following exclusion criteria apply:

    • Age <17 or >80
    • ICU need or indication by the end of the tPA infusion
    • NIHSS >9 at presentation or at the end of the tPA infusion
    • Indication/need for endovascular recanalization therapy

Sites / Locations

  • The Johns Hopkins Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

"Hopkins" post tPA monitoring protocol

Arm Description

Patients treated with IV tPA (intravenous tissue Plasminogen Activator) for acute stroke will be monitored in a non-ICU setting following the "Hopkins" post tPA monitoring protocol, a new schedule for vital signs and neurochecks. These patients will have vital signs and neurochecks every 15 minutes for two hours, then once upon admission to the stroke unit and after one hour, then every two hours for 8 hours and then every four hours until 24 hours post tPA.

Outcomes

Primary Outcome Measures

Number of Participants Needing ICU Care/Interventions Within the First 24 Hours of IV tPA Administration

Secondary Outcome Measures

Severity of Stroke at 24 Hours as Assessed by the National Institutes of Health Stroke Scale (NIHSS)
The NIHSS is a scale of stroke severity with 15 items and a score range from 0 to 42. 0 = no stroke; 1-4 = minor stroke; 5-15 = moderate stroke; 15-20 = moderate/severe stroke; 21-42 = severe stroke.
Degree of Disability as Assessed by the Modified Rankin Score (mRS)
The mRS is a scale of disability with a score range from 0-6. 0 - no symptoms, back to normal. - some symptoms, able to do all prior activities, does not need help from others. - some symptoms, unable to do all prior activities, does not need help from others. - needs help from others, able to walk. - needs help from other, unable to walk without help. - needs total care. - the patient has expired.
Severity of Symptoms of Stroke at 90 Days as Assessed by the NIHSS
The NIHSS is a scale of stroke severity with 15 items and a score range from 0 to 42. 0 = no stroke; 1-4 = minor stroke; 5-15 = moderate stroke; 15-20 = moderate/severe stroke; 21-42 = severe stroke.
Degree of Disability at 90 Days as Assessed by the mRS
The mRS is a scale of disability with a score range from 0-6. 0-no symptoms, back to normal. some symptoms, able to do all prior activities, does not need help from others. some symptoms, unable to do all prior activities, does not need help from others. needs help from others, able to walk. needs help from other, unable to walk without help. needs total care. the patient has expired.
Mortality at 90 Days

Full Information

First Posted
January 16, 2014
Last Updated
March 4, 2020
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT02039375
Brief Title
Safety Study of Post Intravenous tPA Monitoring in Ischemic Stroke
Acronym
OPTIMIST
Official Title
Optimal Post Tpa-Iv Monitoring in Ischemic STroke
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
March 1, 2014 (Actual)
Primary Completion Date
March 21, 2018 (Actual)
Study Completion Date
June 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Intravenous (IV) tissue plasminogen activator (tPA) is the only FDA-approved therapy for treatment of acute ischemic stroke. In the United States, IV tPA is typically administered in the Emergency Department (ED) for patients presenting with acute ischemic stroke within 4.5 hours of symptom onset. It is current practice that post-tPA patients are monitored in an intensive care unit or intensive care unit (ICU)-like setting for at least 24 hours, in part due to frequent vital sign and neurological monitoring that is currently the standard of care. However, rigorous evidence to support this practice is largely lacking. In a retrospective analysis of 153 patients receiving IV tPA at Johns Hopkins Hospital (JHH) and Johns Hopkins Bayview Medical Center (JHBMC), investigators have shown that most patients who have ICU needs in the first 24 hours after tPA administration develop such needs by the end of the tPA infusion. Patients without ICU needs by the end of the tPA infusion, do not require further ICU resources if patients' presenting NIH Stroke Scale (NIHSS) is below 10. This study is a prospective clinical trial that aims at establishing the first proof-of-concept and feasibility of whether patients with a low NIHSS (NIHSS 9 or less) and that do not need ICU care by the end of the tPA infusion, can be monitored safely in a non-ICU setting with a novel monitoring protocol. Identifying post-tPA patients who can be safely monitored in a non-ICU environment may improve cost-effective utilization of ICU resources and reduce the length of hospitalization for stroke patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Ischemic Stroke
Keywords
IV tPA, Thrombolysis, Stroke, Ischemic, Monitoring

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single arm study
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
"Hopkins" post tPA monitoring protocol
Arm Type
Experimental
Arm Description
Patients treated with IV tPA (intravenous tissue Plasminogen Activator) for acute stroke will be monitored in a non-ICU setting following the "Hopkins" post tPA monitoring protocol, a new schedule for vital signs and neurochecks. These patients will have vital signs and neurochecks every 15 minutes for two hours, then once upon admission to the stroke unit and after one hour, then every two hours for 8 hours and then every four hours until 24 hours post tPA.
Intervention Type
Other
Intervention Name(s)
"Hopkins" post tPA for ischemic stroke monitoring protocol
Intervention Description
The "Hopkins" post tPA monitoring protocol includes: vital signs and neurochecks, per standard of care for the first two hours (every 15 minutes), then on arrival to unit, in one hour, every 2 hours for 8 hours, and every 4 hours to complete 24 hours.
Primary Outcome Measure Information:
Title
Number of Participants Needing ICU Care/Interventions Within the First 24 Hours of IV tPA Administration
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Severity of Stroke at 24 Hours as Assessed by the National Institutes of Health Stroke Scale (NIHSS)
Description
The NIHSS is a scale of stroke severity with 15 items and a score range from 0 to 42. 0 = no stroke; 1-4 = minor stroke; 5-15 = moderate stroke; 15-20 = moderate/severe stroke; 21-42 = severe stroke.
Time Frame
24 hours
Title
Degree of Disability as Assessed by the Modified Rankin Score (mRS)
Description
The mRS is a scale of disability with a score range from 0-6. 0 - no symptoms, back to normal. - some symptoms, able to do all prior activities, does not need help from others. - some symptoms, unable to do all prior activities, does not need help from others. - needs help from others, able to walk. - needs help from other, unable to walk without help. - needs total care. - the patient has expired.
Time Frame
At the time of discharge from the hospital, up to 90 days
Title
Severity of Symptoms of Stroke at 90 Days as Assessed by the NIHSS
Description
The NIHSS is a scale of stroke severity with 15 items and a score range from 0 to 42. 0 = no stroke; 1-4 = minor stroke; 5-15 = moderate stroke; 15-20 = moderate/severe stroke; 21-42 = severe stroke.
Time Frame
At 90 days
Title
Degree of Disability at 90 Days as Assessed by the mRS
Description
The mRS is a scale of disability with a score range from 0-6. 0-no symptoms, back to normal. some symptoms, able to do all prior activities, does not need help from others. some symptoms, unable to do all prior activities, does not need help from others. needs help from others, able to walk. needs help from other, unable to walk without help. needs total care. the patient has expired.
Time Frame
At 90 days
Title
Mortality at 90 Days
Time Frame
90 days

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: Ability to provide written informed consent (or a Legally Authorized Representative (LAR) available to provide informed consent) and comply with study assessments for the full duration of the study. Age 18-80 years Patients to be included will be diagnosed as having an acute ischemic stroke by history and physical exam and receive IV tPA within 4.5 hours of symptom onset according to current guidelines for acute stroke care. NIHSS at presentation <10 Patients do not have ICU needs in the judgment of the treating ED physician or neurologist by the end of the tPA infusion NIHSS at the end of tPA infusion <10 Exclusion Criteria: For patients receiving IV tPA according to the current standard of care, the following exclusion criteria apply: Age <17 or >80 ICU need or indication by the end of the tPA infusion NIHSS >9 at presentation or at the end of the tPA infusion Indication/need for endovascular recanalization therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor C Urrutia, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24533130
Citation
Faigle R, Sharrief A, Marsh EB, Llinas RH, Urrutia VC. Predictors of critical care needs after IV thrombolysis for acute ischemic stroke. PLoS One. 2014 Feb 12;9(2):e88652. doi: 10.1371/journal.pone.0088652. eCollection 2014.
Results Reference
background
PubMed Identifier
31839859
Citation
Faigle R, Butler J, Carhuapoma JR, Johnson B, Zink EK, Shakes T, Rosenblum M, Saheed M, Urrutia VC. Safety Trial of Low-Intensity Monitoring After Thrombolysis: Optimal Post Tpa-Iv Monitoring in Ischemic STroke (OPTIMIST). Neurohospitalist. 2020 Jan;10(1):11-15. doi: 10.1177/1941874419845229. Epub 2019 May 5.
Results Reference
result
Links:
URL
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0088652
Description
Preliminary work

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Safety Study of Post Intravenous tPA Monitoring in Ischemic Stroke

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