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A Trial of Low-dose Adjunctive alTeplase During prIMary PCI (T-TIME)

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ClinicalTrials.gov Identifier: NCT02257294
Recruitment Status : Active, not recruiting
First Posted : October 6, 2014
Last Update Posted : May 16, 2018
Sponsor:
Collaborators:
University of Glasgow
National Institute for Health Research, United Kingdom
Information provided by (Responsible Party):
NHS Greater Glasgow and Clyde

Brief Summary:
The purpose of this study is to determine the safety and efficacy of reduced doses (10 mg and 20 mg) of intra-coronary alteplase compared with placebo as an adjunct to PCI in reducing MVO and its consequences in high risk patients with STEMI.

Condition or disease Intervention/treatment Phase
Myocardial Infarction Drug: Alteplase Other: Placebo Phase 2

Detailed Description:
Despite numerous interventions, there remains a need to develop new ways to prevent microvascular obstruction (MVO). The investigators aim to select patients with persistent S-T-elevation on the ECG and an occluded artery and heavy thrombus burden at initial angiography. These characteristics are causally linked to MVO. Patients with a thrombotic culprit coronary artery have reduced myocardial perfusion compared to those without and the presence of coronary thrombus is an independent predictor of adverse ischaemic outcomes post-MI. Intra-luminal thrombus, as revealed by intra vascular imaging with optical coherence tomography (OCT) in STEMI patients, has shown that thrombus commonly persists in the culprit coronary artery, including within the stent post-implantation, even when the thrombus is invisible with conventional angiography. The amount of persistent thrombus predicted the likelihood of persistent S-T-segment elevation, a marker of microvascular injury, and impaired perfusion.Therefore, coronary thrombus represents a therapeutic target in primary PCI. The pathophysiology of MVO and microvascular thrombosis has elucidated in MRI studies of reperfused MI in swine. The investigators demonstrated that LATE MVO corresponds closely with infarct zone haemorrhage as revealed by T2-weighted MRI and pathology. The investigators observations were validated by Robbers et al who showed that in swine 7 days post-MI, when LATE MVO and haemorrhage correspond (which is usually the case), there is severe capillary loss and disruption coupled with thrombosis and inflammation. They concluded that following reperfusion, acute inflammation and microvessel thrombosis result in degradation of endothelial integrity and capillary breakdown. Very interestingly, their histology also demonstrated diffuse microvascular thrombosis within the area of late gadolinium enhancement surrounding the haemorrhagic core which explains reduced perfusion (or wash during first pass of gadolinium contrast MRI) within the ischaemic area-at-risk. This observation points to the therapeutic potential of local thrombolysis within the culprit artery circulation.The study addresses the question of whether a pharmacological strategy involving reduced dose alteplase given early during the primary PCI procedure will both prevent and treat distal microvascular thrombosis and MVO and, subsequently, reduce infarct size.Current evidence around the potential safety and efficacy of reduced dose fibrinolysis in primary PCI is limited. These limitations set-the-scene and support the rationale for the clinical trial: Full systemic dose intravenous fibrinolysis to facilitate primary PCI is potentially harmful and increases the risk of off-target bleeding complications; therefore, the investigators will use reduced-dose fibrinolysis. They will directly infuse alteplase into the culprit artery to achieve effective and sustained local plasma concentrations and much lower systemic concentrations of unbound drug. It is anticipated that bleeding rates may be low; therefore, the investigators will measure fibrinogen in all patients. Fibrinogen and other haemostasis parameters will serve as a surrogate measure of bleeding (and safety). In line with contemporary practice, investigators advise that patients have radial artery access whenever possible. Previous trials have used streptokinase (non-fibrin specific and immunogenic); this study will use the fibrin-specific non-immunogenic second generation thrombolytic, alteplase The only previous trial involved thrombolysis at the end of primary PCI (when microvascular thrombosis may already be established after reperfusion); the efficacy of thrombolysis may be greatest when thrombus is most abundant at the beginning of primary PCI; persistent residual fibrin strands adherent within the culprit territory will be selectively targeted by fibrinolytic therapy during primary PCI; thrombus which forms during the primary PCI procedure could be treated by the sustained 'deep tissue' thrombolytic effects of locally administered intra-coronary alteplase; in terms of ease-of-use and feasibility, there may be advantages to giving alteplase as a single dose.T-TIME is a Phase II evaluation of two reduced doses of alteplase, delivered locally, compared to placebo in STEMI patients receiving PCI in a double-blind, randomised, parallel group, placebo-controlled dose-ranging clinical trial. The investigators believe the strategy with intracoronary fibrinolysis complements other therapeutic approaches which are currently being tested. Should the trial demonstrate EFFICACY then a future trial might involve a factorial design with placebo, alteplase and any other intervention that might also be shown to be effective in the intervening time in order to test the comparative EFFICACY of each (alone or in combination) on surrogate and/or clinical outcomes.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 440 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: A Randomised, Double Blind, Placebo-controlled, Parallel Group Trial of Low-dose Adjunctive alTeplase During prIMary PCI
Actual Study Start Date : March 2016
Estimated Primary Completion Date : June 2018
Estimated Study Completion Date : December 2020

Resource links provided by the National Library of Medicine

Drug Information available for: Alteplase

Arm Intervention/treatment
Placebo Comparator: Control Arm
two placebo vials
Other: Placebo
Single treatment consisting of a single slow infusion administration after reperfusion with aspiration thrombectomy ± angioplasty but before stenting during primary PCI.

Active Comparator: Arm A
Alteplase 10mg and placebo vial
Drug: Alteplase
Single treatment consisting of a single slow infusion administration after reperfusion with aspiration thrombectomy ± angioplasty but before stenting during primary PCI.
Other Name: Actilyse

Other: Placebo
Single treatment consisting of a single slow infusion administration after reperfusion with aspiration thrombectomy ± angioplasty but before stenting during primary PCI.

Active Comparator: Arm B
Alteplase 10mg and alteplase 10mg
Drug: Alteplase
Single treatment consisting of a single slow infusion administration after reperfusion with aspiration thrombectomy ± angioplasty but before stenting during primary PCI.
Other Name: Actilyse




Primary Outcome Measures :
  1. The amount of MVO (% of Left Ventricular (LV) mass) revealed by late (10 - 15 min) gadolinium contrast enhancement MRI 2 days post-MI. [ Time Frame: 2-7 days ]
    Amount of MVO (% of LV mass) revealed by late gadolinium contrast-enhanced MRI 10-15 minutes after contrast administration on an MRI scan performed 2-7 days post-MI.


Secondary Outcome Measures :
  1. Angiogram [ Time Frame: 0-2 hours ]
    TIMI Coronary flow grade at the end of PCI; TIMI blush grade at the end of PCI; TIMI frame count at the end of PCI; TIMI thrombus grade at the end of PCI

  2. ECG [ Time Frame: 0-2 hours ]
    % ST segment resolution on the 12-lead ECG (pre- vs. 60 mins post-reperfusion with primary PCI)

  3. Haematology [ Time Frame: 24 hours ]
    Coagulation

  4. MRI [ Time Frame: 2-7 days ]
    Late MVO (presence/absence); Infarct size; Myocardial salvage index (infarct size/area-at-risk); LV end-diastolic volume (LVEDV); LV end-systolic volume (LVESV); LV ejection fraction (LVEF); Myocardial haemorrhage (presence/absence); Myocardial haemorrhage extent (% of LV)

  5. Safety [ Time Frame: 2-7 days ]
    Acute cerebral (stroke) and systemic (GI, peripheral) bleeding (if any) with alteplase; Coagulation (fibrinogen concentration);

  6. MRI [ Time Frame: 12 weeks ]
    Infarct size; Myocardial salvage index (final infarct size/initial area-at-risk); LV end-diastolic volume (LVEDV); LV end-systolic volume (LVESV); LV ejection fraction (LVEF);

  7. ECG [ Time Frame: 12 weeks ]
    ECG for final infarct size

  8. Biochemistry [ Time Frame: 12 weeks ]
    Troponin T; NT-pro BNP

  9. Quality of Life [ Time Frame: 12 weeks ]
    EQ5D-5L assessment (2-7 days, 12 weeks)


Other Outcome Measures:
  1. Histopathology (sub-study) [ Time Frame: 0 hours ]
    Fibrin histopathology in thrombus aspirate

  2. Angiogram [ Time Frame: 0-2 hours ]
    Intra-procedural changes in TIMI Coronary Flow Grade; Intra-procedural changes in TIMI blush grade; Intra-procedural changes in TIMI Frame Count; Intra-procedural changes in TIMI Thrombus Grade; Intra-procedural thrombotic events

  3. Coronary Physiology (sub-study) [ Time Frame: 0-2 hours ]
    IMR; CFR

  4. Optical Coherence Tomography (sub-study) [ Time Frame: 0-2 hours ]
    Thrombus area

  5. Biochemistry [ Time Frame: 24 hours ]
    Blood chemistry (standard of care blood tests)

  6. Haematology [ Time Frame: 24 hour ]
    Haemoglobin (standard of care blood tests)

  7. Safety [ Time Frame: 24 hours ]
    Haemoglobin (standard of care blood tests)

  8. ECG [ Time Frame: 12 weeks ]
    Surrogate ECG measures of infarct size - Anderson ST Acuteness score and Selvester QRS score; Acuteness of the ECG changes - Anderson Wilkins score;

  9. MRI [ Time Frame: 12 weeks ]
    First pass MVO extent (% of LV); Early MVO extent (% of LV) on 1 min post-gadolinium contrast enhanced MRI , adjusted for area-at-risk at baseline; LV remodelling index (minimum infarct wall thickness / maximum remote zone thickness mid-diastole); LV diastolic myocardial wall thickness to volume; LV sphericity index at end diastole (maximal longitudinal LV diameter (i.e. tip mitral valve to LV index) / maximal short-axis diameter); LV sphericity index at end-systole (maximal longitudinal LV diameter (i.e. tip mitral valve to LV apex) / maximal short-axis diameter); LV wall motion; Myocardial strain; Myocardial haemorrhage; Myocardial perfusion in the infarct zone; Myocardial perfusion in the remote zone; Infarct zone perfusion indexed to remote zone perfusion; Extracellular volume in the infarct zone; Extracellular volume in the remote zone; Extracellular in the infarct core; LV wall motion;

  10. Quality of life [ Time Frame: 2 years ]
    Blood chemistry (standard of care blood tests); EQ5D-5L (52 weeks)

  11. Health outcomes [ Time Frame: 3 years ]
    Death; MI; Heart Failure; Stroke/TIA; Acute bleeds



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Males aged ≥ 18 years; females ≤ 18 years not of child bearing potential (defined as women who are post-menopausal or permanently sterilised (e.g. hysterectomy, tubal occlusion, bilateral salpingectomy)
  • Acute myocardial infarction (symptoms onset ≤ 6 hours) with persistent ST-segment elevation or recent left bundle branch block
  • Coronary artery occlusion (TIMI coronary flow grade 0 or 1) OR Impaired coronary flow (TIMI flow grade 2, slow but complete filling) in the presence of definite angiographic evidence of thrombus (TIMI grade 2+)
  • Proximal-mid culprit lesion location in a major coronary artery (ie the right, left anterior descending, intermediate or circumflex coronary artery)
  • Radial artery access

Exclusion Criteria:

  • Shock (systolic blood pressure <90 mmHg with clinical signs of peripheral hypoperfusion despite adequate filling)
  • Normal coronary flow grade (TIMI flow grade 3) at initial angiography
  • Functional coronary collateral supply (Rentrop grade 2/3) to culprit artery
  • Multivessel PCI intended before the day 2-7 MRI Scan
  • Non-cardiac co-morbidity with expected survival <1 year
  • Estimated body weight <60kg
  • Contra-indication to contrast-enhanced MRI
  • Pacemaker
  • Implantable defibrillator
  • estimated Glomerular Filtration Rate (eGFR) <30ml/min/1.73m²
  • previous infarction in the culprit artery (known or suspected clinically, e.g. wall motion abnormality revealed by echocardiography)
  • Significant bleeding problem either at present or within the past 6 months
  • Patients with current concomitant oral anticoagulant therapy (INR > 1.3), including apixaban, dabigatran and rivaroxaban
  • Any history of central nervous system damage (i.e. neoplasm, aneurysm, intracranial, or spinal surgery)
  • Known Haemorrhagic diathesis
  • Severe uncontrolled hypertension >180/110 mmHg not controlled by medical therapy
  • Major surgery, biopsy of a parenchymal organ, or significant trauma within the past 2 months (this includes any trauma associated with the current STEMI)
  • Recent trauma to the head or cranium (<2 months)
  • Prolonged cardiopulmonary resuscitation (>2 minutes) within past 2 weeks
  • Acute pericarditis and/or subacute bacterial endocarditis e.g. valve mass or vegetation revealed by echocardiography
  • Acute pancreatitis
  • Severe hepatic dysfunction, including hepatic failure, cirrhosis, portal hypertension (oesophageal varices) and active hepatitis
  • Arterial aneurysm and known arterial/venous malformation
  • Neoplasm with increased bleeding risk
  • Any known history of haemorrhagic stroke or stroke of unknown origin
  • Known history of ischaemic stroke or transient ischaemic attack <6 months
  • Dementia
  • Hypersensitivity to gentamicin
  • Women of child-bearing potential (i.e. pre-menopause) or breast feeding
  • Previous randomisation to this study or participation in a study with an investigational drug or medical device within 90 days prior to randomisation
  • Incapacity or inability to provide informed consent
  • requirement for immunosuppressive drug therapy at any time during the past 3 months; whether administered orally, subcutaneously or intravenously. This would include corticosteroids (but not inhaled or topical), drugs used following transplantation (e.g. tacrolimus, cyclosporine), anti-metabolite therapies (e.g. mycophenolic acid (Myfortic), azathioprine, leflunomide (Arava)), and immunomodulators including biologics (e.g. adalimumab (HUMIRA), etanercept (Enbrel), aldesleukin), and DMARDS (cyclophosphamide. methotrexate, etc). Please note that this list is not exhaustive and a requirement for other immunosuppressive drugs not listed would also exclude the patient.
  • active or prophylactic treatment with oral or parenteral antibiotic, antifungal or antiviral therapy to prevent or treat infection.
  • any anti-cancer treatment (excluding surgery as this is covered above) at any time during the past 3 months including chemotherapy, radiotherapy and treatment with biologics such as Vascular Endothelial Growth Factor Receptor (VEGFR) inhibitors (e.g. bevacizumab, pazopanib). This list is not exhaustive and the sponsor or CI should be contacted for advice if required.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02257294


Locations
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United Kingdom
Edinburgh Royal Infirmary
Edinburgh, United Kingdom
Golden Jubilee National Hospital
Glasgow, United Kingdom, G81 4HX
Leeds General Infirmary
Leeds, United Kingdom, LS1 3EX
Glenfield Hospital
Leicester, United Kingdom
Liverpool Heart and Chest Hospital
Liverpool, United Kingdom
Barts Health Centre, St Bartholomew's Hospital
London, United Kingdom, EC1A 7BE
University Hospital of South Manchester NHS Foundation Trust
Manchester, United Kingdom, M23 9LT
James Cook University Hospital
Middlesbrough, United Kingdom
Freeman Hospital
Newcastle, United Kingdom, NE7 7DN
University Hospital Southampton NHS Foundation Trust
Southampton, United Kingdom, SO16 6TD
Heart and Lung Centre, New Cross Hospital
Wolverhampton, United Kingdom, WV10 0QP
Sponsors and Collaborators
NHS Greater Glasgow and Clyde
University of Glasgow
National Institute for Health Research, United Kingdom
Investigators
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Principal Investigator: Colin Berry, Prof University of Glasgow

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: NHS Greater Glasgow and Clyde
ClinicalTrials.gov Identifier: NCT02257294     History of Changes
Other Study ID Numbers: GN12CA450
12/170/45 ( Other Grant/Funding Number: EME )
First Posted: October 6, 2014    Key Record Dates
Last Update Posted: May 16, 2018
Last Verified: May 2018

Additional relevant MeSH terms:
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Infarction
Myocardial Infarction
Ischemia
Pathologic Processes
Necrosis
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Tissue Plasminogen Activator
Fibrinolytic Agents
Fibrin Modulating Agents
Molecular Mechanisms of Pharmacological Action