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TPA in Acute Stroke With COVID Verus Non-COVID-19 Patients (rTPA)

Primary Purpose

Acute Ischemic Stroke

Status
Completed
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
IV tPA (Activase)
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Ischemic Stroke

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Clinically diagnosed as acute ischemic stroke NIHSS<25
  • Symptoms onset less than 4.5 hours (3hours in diabetic or having a previous stroke) before beginning treatment.

Exclusion Criteria:

  • History of:

    • A previous ischemic stroke or severe head trauma in previous 3 months.
    • Previous intracranial hemorrhage .
    • Intracranial neoplasm or gastrointestinal malignancy.
    • Gastrointestinal hemorrhage in previous 3weeks.
    • Intracranial or intra spinal surgery in previous 3months

Clinically:

  • Symptoms suggestive of subarachnoid hemorrhage.
  • Persistent blood pressure elevation, systolic > 185 or diastolic >110 mmHg.
  • Active internal bleeding.
  • Presentations consistent with infective endocarditis.
  • Stroke known or suspected to be associated with aortic arch dissection.
  • Acute bleeding diathesis, including but not limited to conditions defined under hematologic.

Hematologic:

  • Platelet count <100.000 \ mm3
  • Current anticoagulant use with INR>1.7 or PT>15sec or PTT> 40sec.
  • Therapeutic doses of low molecular weight received in 24 hours (not include the prophylactic doses).

Head CT:

  • Evidence of hemorrhage.
  • Extensive regions of obvious hypo density

Sites / Locations

  • Assiut University Hospital
  • Aswan University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

acute ischemic stroke without covid -19 infection

acute ischemic stroke associated with covid -19 infection

Arm Description

Administration of IV tPA: the dose of activase is ,9 mg /kg (not exceeding 90 mg total treatment dose) Infused over 90 minutes.

Administration of IV tPA: the dose of activase is, 9 mg /kg (not exceeding 90 mg total treatment dose) Infused over 90 minutes.

Outcomes

Primary Outcome Measures

primary out come
Barthel Index scale BIS (pre-post drug administration and 2 month later)The Barthel includes 10 personal activities: feeding, personal toileting, bathing, dressing and undressing, getting on and off a toilet, controlling bladder, controlling bowel, moving from wheelchair to bed and returning, walking on level surface (or propelling a wheelchair if unable to walk) and ascending and descending stairs. The original Index is a three-item ordinal rating scale completed by a therapist or other observer in 2-5 minutes. Each item is rated in terms of whether the patient can perform the task independently, with some assistance, or is dependent on help based on observation (0=unable, 1=needs help, 2=independent). The final score is x 5 to get a number on a 100 point score. Proposed guidelines for interpreting Barthel scores are that scores of 0-20 indicate "total" dependency, 21-60 indicate "severe" dependency, 61-90 indicate "moderate" dependency, and 91-99 indicates "slight" dependency.

Secondary Outcome Measures

secondary outcome
NIHSS (pre-post drug administration and 2 month later a tool used by healthcare providers to objectively quantify the impairment caused by a stroke. The NIHSS is composed of 11 items( Level of Consciousness ,Horizontal Eye Movement, Visual field test, Facial Palsy, Motor Arm, Motor Leg, Limb Ataxia ,Sensory, Language and Speech) , each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment. The individual scores from each item are summed in order to calculate a patient's total NIHSS score. The maximum possible score is 42, with the minimum score being a 0.Score 0 means No stroke symptoms. score 1-4 means Minor stroke .Score 5-15 means Moderate stroke. score 16-20 means Moderate to severe stroke. Score 21-42 means Severe stroke

Full Information

First Posted
February 21, 2022
Last Updated
October 27, 2022
Sponsor
Assiut University
Collaborators
Aswan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05258565
Brief Title
TPA in Acute Stroke With COVID Verus Non-COVID-19 Patients
Acronym
rTPA
Official Title
Tissue Plasminogen Activator (tPA) Therapy for Acute Ischemic Stroke in Covid -19 and Non Covid -19 Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2022 (Actual)
Primary Completion Date
June 15, 2022 (Actual)
Study Completion Date
September 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Assiut University
Collaborators
Aswan University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigator will recruit consecutively all patients coming with acute ischemic stroke either with or without COVID -19 infection and suitable for IV injection with Tissue plasminogen activators according to guideline and inclusion criteria of tPA. Aswan University Hospital.
Detailed Description
Acute ischemic stroke (AIS) is a time sensitive medical emergency and a leading cause of morbidity and mortality worldwide. Intravenous (IV) recombinant tissue plasminogen activator (IV alteplase) is currently the only proven effective medication for the treatment of AIS with promising adjuvant medications currently under investigation.(Gottula et al, 2021). Intravenous tissue plasminogen activator (tPA) is used to treat acute stroke because of its thrombolytic activity and its ability to restore circulation to the brain. (Wang, et. al, 1998). However tPA administration, especially delayed administration is associated with increased intracranial hemorrhage, hemorrhagic transformation and mortality. (Jong, 2019) Acute cerebrovascular disease, particularly ischemic stroke, has emerged as a serious complication of infection by the severe acute respiratory syndrome coronavirus that caused by the Coronavirus disease-2019 (COVID-19). Such specificities include a propensity towards large vessel occlusion, multi-territory stroke, and involvement of otherwise uncommonly affected vessels. The pathogenesis and optimal management of ischemic stroke associated with COVID-19 still remain uncertain, but emerging evidence suggest that cytokine storm-triggered coagulopathy and endotheliopathy represent possible targetable mechanisms. (Vogrig, et. al, 2021). Anew study was done in United States in 2020, included 13 patients presented with acute ischemic stroke and systemic symptoms consistent with covid-19 were treated with IV tPA. 61.5% of patients improved at follow up, Neither of them complicated with systemic or symptomatic intracranial hemorrhages.(Carneiro, et. al, 2020). IV tPA may be safe and efficacious in COVID -19 but larger studies are needed to validate these results (Carneiro, et. al, 2020). The purpose of this study is to compare between the safety and efficacy of tPA management of ischemic stroke in Covid-19 and non covid-19 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Ischemic Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
acute ischemic stroke without covid -19 infection
Arm Type
Active Comparator
Arm Description
Administration of IV tPA: the dose of activase is ,9 mg /kg (not exceeding 90 mg total treatment dose) Infused over 90 minutes.
Arm Title
acute ischemic stroke associated with covid -19 infection
Arm Type
Active Comparator
Arm Description
Administration of IV tPA: the dose of activase is, 9 mg /kg (not exceeding 90 mg total treatment dose) Infused over 90 minutes.
Intervention Type
Drug
Intervention Name(s)
IV tPA (Activase)
Other Intervention Name(s)
IV tissue plasminogen activator
Intervention Description
Any patients eligible came with acute ischemic stroke with or without COVID-19 infection within the time window for thrombolytic therapy (within 4 hours of onset)
Primary Outcome Measure Information:
Title
primary out come
Description
Barthel Index scale BIS (pre-post drug administration and 2 month later)The Barthel includes 10 personal activities: feeding, personal toileting, bathing, dressing and undressing, getting on and off a toilet, controlling bladder, controlling bowel, moving from wheelchair to bed and returning, walking on level surface (or propelling a wheelchair if unable to walk) and ascending and descending stairs. The original Index is a three-item ordinal rating scale completed by a therapist or other observer in 2-5 minutes. Each item is rated in terms of whether the patient can perform the task independently, with some assistance, or is dependent on help based on observation (0=unable, 1=needs help, 2=independent). The final score is x 5 to get a number on a 100 point score. Proposed guidelines for interpreting Barthel scores are that scores of 0-20 indicate "total" dependency, 21-60 indicate "severe" dependency, 61-90 indicate "moderate" dependency, and 91-99 indicates "slight" dependency.
Time Frame
2 months
Secondary Outcome Measure Information:
Title
secondary outcome
Description
NIHSS (pre-post drug administration and 2 month later a tool used by healthcare providers to objectively quantify the impairment caused by a stroke. The NIHSS is composed of 11 items( Level of Consciousness ,Horizontal Eye Movement, Visual field test, Facial Palsy, Motor Arm, Motor Leg, Limb Ataxia ,Sensory, Language and Speech) , each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment. The individual scores from each item are summed in order to calculate a patient's total NIHSS score. The maximum possible score is 42, with the minimum score being a 0.Score 0 means No stroke symptoms. score 1-4 means Minor stroke .Score 5-15 means Moderate stroke. score 16-20 means Moderate to severe stroke. Score 21-42 means Severe stroke
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinically diagnosed as acute ischemic stroke NIHSS<25 Symptoms onset less than 4.5 hours (3hours in diabetic or having a previous stroke) before beginning treatment. Exclusion Criteria: History of: A previous ischemic stroke or severe head trauma in previous 3 months. Previous intracranial hemorrhage . Intracranial neoplasm or gastrointestinal malignancy. Gastrointestinal hemorrhage in previous 3weeks. Intracranial or intra spinal surgery in previous 3months Clinically: Symptoms suggestive of subarachnoid hemorrhage. Persistent blood pressure elevation, systolic > 185 or diastolic >110 mmHg. Active internal bleeding. Presentations consistent with infective endocarditis. Stroke known or suspected to be associated with aortic arch dissection. Acute bleeding diathesis, including but not limited to conditions defined under hematologic. Hematologic: Platelet count <100.000 \ mm3 Current anticoagulant use with INR>1.7 or PT>15sec or PTT> 40sec. Therapeutic doses of low molecular weight received in 24 hours (not include the prophylactic doses). Head CT: Evidence of hemorrhage. Extensive regions of obvious hypo density
Facility Information:
Facility Name
Assiut University Hospital
City
Assiut
Country
Egypt
Facility Name
Aswan University Hospital
City
Aswan
Country
Egypt

12. IPD Sharing Statement

Links:
URL
https://pubmed.ncbi.nlm.nih.gov/33472270/
Description
• Gottula AL, Barreto AD, Adeoye O. Alteplase and Adjuvant Therapies for Acute Ischemic Stroke. Semin Neurol. 2021 Feb;41(1):16-27. doi: 10.1055/s-0040-1722720. Epub 2021 Jan 20. PMID: 33472270..
URL
https://pubmed.ncbi.nlm.nih.gov/9461198/
Description
• Wang YF, Tsirka SE, Strickland S, Stieg PE, Soriano SG, Lipton SA.Tissue plasminogen activator (tPA) increases neuronal damage after focal cerebral ischemia in wild-type and tPA-deficient mice.
URL
https://pubmed.ncbi.nlm.nih.gov/33352277/
Description
• Vogrig A, Gigli GL, Bnà C, Morassi M. Stroke in patients with COVID-19: Clinical and neuroimaging characteristics. Neurosci Lett. 2021 Jan 19;743:135564. doi: 10.1016/j.neulet.2020.135564. Epub 2020 Dec 19. PMID: 33352277; PMCID: PMC7749733.
URL
https://pubmed.ncbi.nlm.nih.gov/31161761/
Description
• Kim, Jong S. "tPA Helpers in the Treatment of Acute Ischemic Stroke: Are They Ready for Clinical Use?." Journal of stroke vol. 21,2 (2019): 160-174. doi:10.5853/jos.2019.00584
URL
https://scholarlycommons.henryford.com/neurology_articles/478
Description
Intravenous tPA for Acute Ischemic Stroke in Patients with COVID-19. J Stroke Cerebrovasc Dis. 2020 Nov;29(11):105201. doi: 10.1016/j.jstrokecerebrovasdis.2020.105201. Epub 2020 Jul 27. PMID: 33066885; PMCID: PMC7383145.

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TPA in Acute Stroke With COVID Verus Non-COVID-19 Patients

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