search
Back to results

Thrombolysis of Urokinase for Minor Stroke (TRUST)

Primary Purpose

Minor Stroke

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Urokinase thrombolysis
Aspirin;Clopidogrel
Sponsored by
The First Affiliated Hospital of Zhengzhou University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Minor Stroke focused on measuring Thrombolysis, Urokinase, Ischemic stroke

Eligibility Criteria

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

Inclusion Criteria:

  1. Adult patients: 18-80 years old
  2. The time from last seen well to treatment < 6 hours
  3. Minor stroke defined as a baseline NIHSS ≤5 at the time of randomization..
  4. First onset or pre-stroke mRS≤1
  5. Informed consent signed

Exclusion Criteria:

1.Hyperdensity on CT suggesting intracranial hemorrhage

2.Large acute stroke >1/3 middle cerebral artery (MCA) territory visible on CT or MRI

3.Other contraindications of intravenous thrombolysis, including but not limited to:

  1. Intracranial tumor, arteriovenous malformation
  2. Coma or confirmed as severe stroke by clinical assessment (e.g. NIHSS ≥25) or proper imaging methods
  3. With seizure
  4. Stroke attack within past three months
  5. Heparin administration within 48h before onset, with APTT longer than upper limit
  6. Stroke history with diabetes
  7. Platelet count ≤100×10^9/L
  8. Difficult to control hypertension, defined by systolic pressure ≥185mmHg or diastolic pressure ≥110 mmHg in 3 tests with at least ten minutes interval, under well guided medications.
  9. Blood glucose <50mg/dl(2.7mmol/l)or >400mg/dl(22.2mmol/l)
  10. Obvious hemorrhage within past 6 months
  11. Oral anti-coagulation drug administration (e.g. warfarin) with INR>1.5
  12. Intracranial hemorrhage or suspected intracranial hemorrhage (including subarachnoid hemorrhage)
  13. Pregnancy or lactation.
  14. History of severe CNS damage (e.g. tumor, arterial aneurysm or CNS surgery)
  15. Hemorrhagic retinopathy, e.g. diabetes (hemorrhages suggested by optic impairment) or other hemorrhagic ocular lesions.
  16. Bacterial endocarditis or pericarditis.
  17. Prolonged or traumatic CPR (>2min), puncture in nonstress vessels within past 10 days, such as subclavian vein puncture.
  18. Acute pancreatitis.
  19. Confirmed ulcerative gastric or intestinal problems within 3 months.
  20. Arterial aneurysm or arteriovenous malformation.
  21. Any tumor that increase risk of hemorrhage.
  22. Severe hepatic diseases, like hepatic failure, liver cirrhosis, portal hypertension, esophageal varices or active hepatitis.
  23. Major surgery, severe trauma or craniocerebral trauma within past 10 days.
  24. Allergy to any components of urokinase.

4.Severe, fatal diseases with less than 3 month expected survival.

5.Intended to receive standard rt-PA thrombolysis or intravascular therapy.

6.Already participating in other studies that conflict to this study.

7.Unable to accomplish the follow-up.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    Urokinase thrombolysis

    Antiplatelet treatment

    Arm Description

    The patients of intervention group will receive 1 millions units urokinase dissolved by 100 saline through intravenous infusion within 30 minutes.

    The control group will receive antiplatelet agents as decided by the physicians according to Chinese guideline for diagnosis and treatment of acute ischemic stroke 2018

    Outcomes

    Primary Outcome Measures

    Proportion of patients with a modified Rankin Scale(mRS) of 0 or 1 at 90-day follow-up
    mRS has 0-6 points, the higher the worse outcome.
    Proportion of patients with symptomatic intracranial hemorrhage within 36 hours
    Symptomatic intracranial haemorrhage within 36 hours

    Secondary Outcome Measures

    Proportion of patients with new vascular events
    Proportion of patients with new vascular events within 90 days(Ischemic stroke / hemorrhagic stroke / TIA / myocardial infarction / vascular death)
    MRS score
    To evaluate the progress of MRS score
    The ratio of patients with MRS 0-1 during the last visit in two groups
    mRS has 0-6 points, the higher the worse outcome.
    Changes in National Institutes of Health Stroke Scale(NIHSS) score
    Neurological impairment in two groups (changes in NIHSS score at 90-day follow-up). NIHSS has 0-42 points, the higher the worse outcome.
    Barthel index (BI) score
    Daily function evaluations(BI score at 90 days). BI has 0-100 points,the higher the bettter outcome.
    Quality of life assessments
    EuroQol five dimensional questionnaire (EQ-5D scale).
    Overall mortality
    Overall mortality within 90 days
    Adverse events and severe adverse events
    Adverse events and severe adverse events in two groups during 90 days

    Full Information

    First Posted
    June 4, 2020
    Last Updated
    June 8, 2020
    Sponsor
    The First Affiliated Hospital of Zhengzhou University
    Collaborators
    Beijing Tiantan Hospital, Shanghai 10th People's Hospital, General Hospital of Shenyang Military Region
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04420351
    Brief Title
    Thrombolysis of Urokinase for Minor Stroke
    Acronym
    TRUST
    Official Title
    A Phase ⅢB, Prospective, Randomized, Open Label, Blinded-endpoint, Multicenter Trial of the Efficacy and Safety of Urokinase Thrombolysis Comparing With Antiplatelet Agents for Patients With Minor Stroke.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 10, 2020 (Anticipated)
    Primary Completion Date
    September 18, 2021 (Anticipated)
    Study Completion Date
    December 18, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    The First Affiliated Hospital of Zhengzhou University
    Collaborators
    Beijing Tiantan Hospital, Shanghai 10th People's Hospital, General Hospital of Shenyang Military Region

    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
    This trial will enroll patients that have been diagnosed with minor stroke, which has occurred within the past 6 hours. TRUST is a prospective multicenter, randomized, blinded-endpoint study to evaluate the efficacy and safety of Urokinase Thrombolysis for patients with minor stroke.
    Detailed Description
    China is currently faced with the heaviest stroke burden due to the tremendous population and susceptibility to cerebrovascular disease. As has been assessed, deaths caused by cerebrovascular disease are three times of cardiovascular disease. Within whole population with cerebrovascular disease, minor stoke have taken a significant part of the disease burden. Thus the population with minor stoke is one of the most important parts in efficient prevention of cerebrovascular disease. According to phase I and II data from national stoke registration in China, 35.25% to 42.23% cases were minor ischemic strokes. However, in clinical practice, the minor ischemic stroke patients are likely to be ignored and some might have poor prognosis. As has been demonstrated by a number of studies, up to one third of the acute non-disabling ischemic stroke without in-time thrombolysis may suffer from disabling or death at 90-day follow-up. Several studies have demonstrated the potential benefits of thrombolysis compared usually with placebo, including the Third International Stroke Trail ( IST-3, rt-PA to placebo, patients within 3 hours after attack, with blood pressure lower than 185/110mmHg and NIHSS≤5),National Institute of Neurological Disorders and Stroke rt-PA Stroke Study( NINDS, rt-PA to placebo, patients with mild ischemic stroke recognized by 5 different definitions). Urokinase is a kind of non-selective plasminogen activator, urokinase acted as effective catalyzer in the transferring of both free and protein-binding plasminogen to plasmin, thus inducing thrombolysis. As one of the widely used medication for intravenous thrombolysis in China, urokinase has been suggested the the efficacy and safety for ischemic stroke. With easier availability and lower price, urokinase has provided a promising alternation to patients who need thrombolysis in China, especially in less developed areas. The Chinese guideline for diagnosis and treatment of acute ischemic stroke 2018 has recommended urokinase as an alternation in the treatment of acute ischemic stroke within 6-hour time window as well, if rt-PA is not available or affordable. However, randomized and multicenter clinical trial of urokinase thrombolysis for minor stroke is still vacant, which couldn't provide more persuasive evidence. TRUST is a prospective multicenter, randomized, single-blind evaluation study to evaluate the efficacy and safety of Urokinase Thrombolysis for patients with minor stroke. The trail will enroll a total of 1002 minor stroke patients within a 6 hour time window with a NIHSS score ≤5 at the time of randomization. Randomization will be 1:1 to Urokinase Thrombolysis (experimental) or Antiplatelet agents (control). Patients will receive 1 million units urokinase dissolved by 100ml saline through intravenous infusion within 30min or oral antiplatelet agents. All patients will undergo CT or MRI before treatment and will undergo the second CT within 36 hours after treatment. Patients will be followed up at 36h, 7d and 90 days. The primary outcome measures including the proportion of patients with a modified Rankin Scale(mRS) of 0 or 1 at 90-day follow-up and the patients with symptomatic intracranial hemorrhage within 36 hours. Secondary outcome measures cover new vascular events, the Progress of MRS score, Neurological impairment, Daily function evaluations, Quality of life assessments, Overall mortality and Adverse events and severe adverse events within 90 days.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Minor Stroke
    Keywords
    Thrombolysis, Urokinase, Ischemic stroke

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    1002 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Urokinase thrombolysis
    Arm Type
    Experimental
    Arm Description
    The patients of intervention group will receive 1 millions units urokinase dissolved by 100 saline through intravenous infusion within 30 minutes.
    Arm Title
    Antiplatelet treatment
    Arm Type
    Other
    Arm Description
    The control group will receive antiplatelet agents as decided by the physicians according to Chinese guideline for diagnosis and treatment of acute ischemic stroke 2018
    Intervention Type
    Drug
    Intervention Name(s)
    Urokinase thrombolysis
    Other Intervention Name(s)
    Urokinase
    Intervention Description
    The patients of intervention group will receive 1 millions units urokinase dissolved by 100 saline through intravenous infusion within 30 minutes.
    Intervention Type
    Drug
    Intervention Name(s)
    Aspirin;Clopidogrel
    Other Intervention Name(s)
    Antiplatelet treatment
    Intervention Description
    The control group will receive antiplatelet agents as decided by the physicians according to Chinese guideline for diagnosis and treatment of acute ischemic stroke 2018.
    Primary Outcome Measure Information:
    Title
    Proportion of patients with a modified Rankin Scale(mRS) of 0 or 1 at 90-day follow-up
    Description
    mRS has 0-6 points, the higher the worse outcome.
    Time Frame
    90 Days
    Title
    Proportion of patients with symptomatic intracranial hemorrhage within 36 hours
    Description
    Symptomatic intracranial haemorrhage within 36 hours
    Time Frame
    36 hours
    Secondary Outcome Measure Information:
    Title
    Proportion of patients with new vascular events
    Description
    Proportion of patients with new vascular events within 90 days(Ischemic stroke / hemorrhagic stroke / TIA / myocardial infarction / vascular death)
    Time Frame
    90 days
    Title
    MRS score
    Description
    To evaluate the progress of MRS score
    Time Frame
    90 days
    Title
    The ratio of patients with MRS 0-1 during the last visit in two groups
    Description
    mRS has 0-6 points, the higher the worse outcome.
    Time Frame
    90 days
    Title
    Changes in National Institutes of Health Stroke Scale(NIHSS) score
    Description
    Neurological impairment in two groups (changes in NIHSS score at 90-day follow-up). NIHSS has 0-42 points, the higher the worse outcome.
    Time Frame
    90 days
    Title
    Barthel index (BI) score
    Description
    Daily function evaluations(BI score at 90 days). BI has 0-100 points,the higher the bettter outcome.
    Time Frame
    90 days
    Title
    Quality of life assessments
    Description
    EuroQol five dimensional questionnaire (EQ-5D scale).
    Time Frame
    90 days
    Title
    Overall mortality
    Description
    Overall mortality within 90 days
    Time Frame
    90 days
    Title
    Adverse events and severe adverse events
    Description
    Adverse events and severe adverse events in two groups during 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: Adult patients: 18-80 years old The time from last seen well to treatment < 6 hours Minor stroke defined as a baseline NIHSS ≤5 at the time of randomization.. First onset or pre-stroke mRS≤1 Informed consent signed Exclusion Criteria: 1.Hyperdensity on CT suggesting intracranial hemorrhage 2.Large acute stroke >1/3 middle cerebral artery (MCA) territory visible on CT or MRI 3.Other contraindications of intravenous thrombolysis, including but not limited to: Intracranial tumor, arteriovenous malformation Coma or confirmed as severe stroke by clinical assessment (e.g. NIHSS ≥25) or proper imaging methods With seizure Stroke attack within past three months Heparin administration within 48h before onset, with APTT longer than upper limit Stroke history with diabetes Platelet count ≤100×10^9/L Difficult to control hypertension, defined by systolic pressure ≥185mmHg or diastolic pressure ≥110 mmHg in 3 tests with at least ten minutes interval, under well guided medications. Blood glucose <50mg/dl(2.7mmol/l)or >400mg/dl(22.2mmol/l) Obvious hemorrhage within past 6 months Oral anti-coagulation drug administration (e.g. warfarin) with INR>1.5 Intracranial hemorrhage or suspected intracranial hemorrhage (including subarachnoid hemorrhage) Pregnancy or lactation. History of severe CNS damage (e.g. tumor, arterial aneurysm or CNS surgery) Hemorrhagic retinopathy, e.g. diabetes (hemorrhages suggested by optic impairment) or other hemorrhagic ocular lesions. Bacterial endocarditis or pericarditis. Prolonged or traumatic CPR (>2min), puncture in nonstress vessels within past 10 days, such as subclavian vein puncture. Acute pancreatitis. Confirmed ulcerative gastric or intestinal problems within 3 months. Arterial aneurysm or arteriovenous malformation. Any tumor that increase risk of hemorrhage. Severe hepatic diseases, like hepatic failure, liver cirrhosis, portal hypertension, esophageal varices or active hepatitis. Major surgery, severe trauma or craniocerebral trauma within past 10 days. Allergy to any components of urokinase. 4.Severe, fatal diseases with less than 3 month expected survival. 5.Intended to receive standard rt-PA thrombolysis or intravascular therapy. 6.Already participating in other studies that conflict to this study. 7.Unable to accomplish the follow-up.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yongli Tao, MD;PhD
    Phone
    +86-371-66278068
    Email
    tyl2112@126.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yafang Xu, MD
    Phone
    +86-371-66278067
    Email
    yafangxu321@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Bo Song, MD;PhD
    Organizational Affiliation
    The First Affiliated Hospital of Zhengzhou University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    17434100
    Citation
    Liu M, Wu B, Wang WZ, Lee LM, Zhang SH, Kong LZ. Stroke in China: epidemiology, prevention, and management strategies. Lancet Neurol. 2007 May;6(5):456-64. doi: 10.1016/S1474-4422(07)70004-2.
    Results Reference
    background
    PubMed Identifier
    11157701
    Citation
    Wu Z, Yao C, Zhao D, Wu G, Wang W, Liu J, Zeng Z, Wu Y. Sino-MONICA project: a collaborative study on trends and determinants in cardiovascular diseases in China, Part i: morbidity and mortality monitoring. Circulation. 2001 Jan 23;103(3):462-8. doi: 10.1161/01.cir.103.3.462.
    Results Reference
    background
    PubMed Identifier
    22052510
    Citation
    Liu L, Wang D, Wong KS, Wang Y. Stroke and stroke care in China: huge burden, significant workload, and a national priority. Stroke. 2011 Dec;42(12):3651-4. doi: 10.1161/STROKEAHA.111.635755. Epub 2011 Nov 3.
    Results Reference
    background
    PubMed Identifier
    21903949
    Citation
    Smith EE, Fonarow GC, Reeves MJ, Cox M, Olson DM, Hernandez AF, Schwamm LH. Outcomes in mild or rapidly improving stroke not treated with intravenous recombinant tissue-type plasminogen activator: findings from Get With The Guidelines-Stroke. Stroke. 2011 Nov;42(11):3110-5. doi: 10.1161/STROKEAHA.111.613208. Epub 2011 Sep 8.
    Results Reference
    background
    PubMed Identifier
    11320171
    Citation
    Barber PA, Zhang J, Demchuk AM, Hill MD, Buchan AM. Why are stroke patients excluded from TPA therapy? An analysis of patient eligibility. Neurology. 2001 Apr 24;56(8):1015-20. doi: 10.1212/wnl.56.8.1015.
    Results Reference
    background
    PubMed Identifier
    17673713
    Citation
    Nedeltchev K, Schwegler B, Haefeli T, Brekenfeld C, Gralla J, Fischer U, Arnold M, Remonda L, Schroth G, Mattle HP. Outcome of stroke with mild or rapidly improving symptoms. Stroke. 2007 Sep;38(9):2531-5. doi: 10.1161/STROKEAHA.107.482554. Epub 2007 Aug 2.
    Results Reference
    background
    PubMed Identifier
    16210552
    Citation
    Smith EE, Abdullah AR, Petkovska I, Rosenthal E, Koroshetz WJ, Schwamm LH. Poor outcomes in patients who do not receive intravenous tissue plasminogen activator because of mild or improving ischemic stroke. Stroke. 2005 Nov;36(11):2497-9. doi: 10.1161/01.STR.0000185798.78817.f3. Epub 2005 Oct 6.
    Results Reference
    background
    PubMed Identifier
    25677596
    Citation
    Coutts SB, Dubuc V, Mandzia J, Kenney C, Demchuk AM, Smith EE, Subramaniam S, Goyal M, Patil S, Menon BK, Barber PA, Dowlatshahi D, Field T, Asdaghi N, Camden MC, Hill MD; TEMPO-1 Investigators. Tenecteplase-tissue-type plasminogen activator evaluation for minor ischemic stroke with proven occlusion. Stroke. 2015 Mar;46(3):769-74. doi: 10.1161/STROKEAHA.114.008504. Epub 2015 Feb 12.
    Results Reference
    background
    PubMed Identifier
    26106113
    Citation
    Khatri P, Tayama D, Cohen G, Lindley RI, Wardlaw JM, Yeatts SD, Broderick JP, Sandercock P; PRISMS and IST-3 Collaborative Groups. Effect of Intravenous Recombinant Tissue-Type Plasminogen Activator in Patients With Mild Stroke in the Third International Stroke Trial-3: Post Hoc Analysis. Stroke. 2015 Aug;46(8):2325-7. doi: 10.1161/STROKEAHA.115.009951. Epub 2015 Jun 23.
    Results Reference
    background
    PubMed Identifier
    16126134
    Citation
    National Institute of Neurological Disorders Stroke rt-PA Stroke Study Group. Recombinant tissue plasminogen activator for minor strokes: the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study experience. Ann Emerg Med. 2005 Sep;46(3):243-52. doi: 10.1016/j.annemergmed.2005.02.013.
    Results Reference
    background
    PubMed Identifier
    20814000
    Citation
    Khatri P, Kleindorfer DO, Yeatts SD, Saver JL, Levine SR, Lyden PD, Moomaw CJ, Palesch YY, Jauch EC, Broderick JP. Strokes with minor symptoms: an exploratory analysis of the National Institute of Neurological Disorders and Stroke recombinant tissue plasminogen activator trials. Stroke. 2010 Nov;41(11):2581-6. doi: 10.1161/STROKEAHA.110.593632. Epub 2010 Sep 2.
    Results Reference
    background

    Learn more about this trial

    Thrombolysis of Urokinase for Minor Stroke

    We'll reach out to this number within 24 hrs