A Study of Low-dose Intracoronary Thrombolytic Therapy in STEMI (Heart Attack) Patients. (RESTORE-MI)
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| ClinicalTrials.gov Identifier: NCT03998319 |
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Recruitment Status :
Recruiting
First Posted : June 26, 2019
Last Update Posted : January 20, 2023
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Sponsor:
University of Sydney
Collaborator:
Genentech, Inc.
Information provided by (Responsible Party):
University of Sydney
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Brief Summary:
Heart attacks are caused by a blood clot blocking the blood vessels of the heart, preventing blood getting to the heart muscle. Opening up the artery with a balloon (angioplasty) and a small mesh tube (stent) although life saving can cause this clot to break up and get washed downstream, which can make the heart attack worse. The investigators can measure the amount of damage caused to the microcirculation by calculating the IMR (Index of Microcirculatory resistance).
This can be measured by a wire in the coronary artery with a pressure sensor at the tip. If the IMR is elevated, it is suggestive of extensive microcirculatory damage. A clot dissolving medicine can be administered in the artery to try and reduce the IMR which can reduce damage to the heart muscle and improve outcomes.
Impaired microcirculatory perfusion in patients as a result of ST-elevation myocardial infarction (STEMI) is associated with poor clinical outcomes. This project seeks to identify patients with impaired microcirculatory perfusion after STEMI and to assess whether acute improvement in microcirculatory perfusion in these patients by the use of intracoronary thrombolytic therapy results in improved clinical outcomes.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| STEMI Elevated IMR (>32) | Drug: Tenecteplase (1/3 systemic weight based dose) Other: Sterile water for injection (WFI) Drug: Tenecteplase (1/6 systemic weight based dose) | Phase 3 |
Patients presenting to the participating hospitals with a heart attack will be approached to participate in the study. After angioplasty has been performed, the IMR will be measured in the infarct related artery. If the IMR is >32 patients will be randomised to receive intracoronary clot dissolving therapy in the form of low, or very low dose tenecteplase (TNK) or water as a placebo. Patients who have an IMR ≤32 will be followed up in a registry. Cardiac enzymes will be measured at baseline and discharge. Randomised participants will receive a cardiac MRI at discharge (3-7 days post primary PCI) and at 6 months post PCI. All participants will be followed up at 30 days, and 6, 12 and 24 months following discharge.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 506 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Multi-Centre double-blind, placebo controlled randomised phase IIIb clinical trial, stratified and balanced between groups on important prognostic factors. |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Masking Description: | All parties involved will be blinded. |
| Primary Purpose: | Other |
| Official Title: | A Randomised Trial to Evaluate the Efficacy of Low-dose Intracoronary Tenecteplase in ST-Elevation Myocardial Infarction (STEMI) Patients With High Microvascular Resistance Post-percutaneous Coronary Intervention (PCI). |
| Actual Study Start Date : | October 14, 2021 |
| Estimated Primary Completion Date : | December 31, 2023 |
| Estimated Study Completion Date : | December 31, 2025 |
Resource links provided by the National Library of Medicine
MedlinePlus related topics:
Heart Attack
Drug Information available for:
Tenecteplase
| Arm | Intervention/treatment |
|---|---|
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Experimental: Tenecteplase (1/3 systemic weight based dose)
Tenecteplase will be reconstituted in 20mL sterile water for injection at 1/3 of the weight based dose, and administered by intracoronary infusion over 3 minutes.
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Drug: Tenecteplase (1/3 systemic weight based dose)
50mg reconstituted to 20mL for intracoronary infusion at 1/3 weight based dose.
Other Name: TNKase |
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Placebo Comparator: Sterile Water for injection (WFI)
Water for injection will be prepared to 20mL over an equivalent time period to the reconstitution time of the experimental arm, in order to maintain the blind, and administered by intracoronary infusion over 3 minutes.
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Other: Sterile water for injection (WFI)
Placebo comparative arm. |
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Experimental: Tenecteplase (1/6 systemic weight based dose)
Tenecteplase will be reconstituted in 20mL sterile water for injection at 1/6 of the weight based dose, and administered by intracoronary infusion over 3 minutes.
|
Drug: Tenecteplase (1/6 systemic weight based dose)
50mg reconstituted to 20mL for intracoronary infusion at 1/6 weight based dose.
Other Name: TNKase |
Primary Outcome Measures :
- To compare the number of participants who experience cardiovascular mortality and rehospitalisation for heart failure at 24 months in those given tenecteplase with those given placebo (Dose Finding and Cardiac MRI cohort only) [ Time Frame: 24 months ]Cardiovascular mortality and rehospitalisation for heart failure assessed by medical record review.
- To compare MI size as a % of LV mass and intramyocardial bleeding rates in participants at 6 months post PCI in those given tenecteplase (low and very low doses) with those given placebo. [ Time Frame: 6 months after primary PCI procedure. ]MI size and intramyocardial bleeding rates will be assessed upon cardiac MRI at discharge (3-7 days post procedure) as a baseline measure, and at 6 months post-PCI.
Secondary Outcome Measures :
- Number of participants who experience individual components of the primary endpoint: (a) cardiovascular mortality at 24 months, (b) rehospitalisation for heart failure at 24 months; [ Time Frame: 24 months after primary PCI procedure ]Cardiovascular mortality and rehospitalisation for heart failure assessed by medical record review, respectively.
- Number of Major Adverse Cardiac Events (MACE) [ Time Frame: 24 months after primary PCI procedure ]Major Adverse Coronary Events (these are combination events involving cardiovascular death, non-fatal MI, non-fatal stroke and unstable angina) assessed from physical assessment and medical record review
- All-cause mortality [ Time Frame: 24 months after primary PCI procedure ]All-cause mortality assessed by physical assessment and medical record review.
- Number of stroke events [ Time Frame: 24 months after primary PCI procedure ]Stroke events will be assessed by medical record review. Assessment will cover all aspects of the stroke event (including type, severity, frequency).
- Number of incidences of bailout treatment use for no-reflow syndrome [ Time Frame: 24 months after primary PCI procedure ]Use of Bailout treatment for no-reflow syndrome assessed by medical record review
- Occurrence of major (Type 3 or greater) and minor (Type 2) bleeding as defined by the Bleeding Academic Research Consortium [ Time Frame: 24 months after primary PCI procedure ]Major (Type 3 or greater) and minor (Type 2) bleeding as defined by the Bleeding Academic Research Consortium. Assessed by medical record review.
- Index of Microcirculatory Resistance (IMR) [ Time Frame: 0-2 hours ]
Index of microcirculatory resistance (IMR) measurement assessed by coronary pressure wire data output review.
This is a simple unit scale, with a higher number indicating a worse outcome with a score of more than 25 indicating abnormal microcirculatory function in the heart.
- Fractional Flow Reserve (FFR) [ Time Frame: 0-2 hours ]Fractional Flow Reserve measurement assessed by coronary pressure wire data output review prior to randomisation and immediately after primary PCI
- Coronary Flow Reserve (CFR) [ Time Frame: 0-2 hours ]Coronary Flow Reserve measurement assessed by coronary pressure wire data output review, prior to randomisation and immediately after primary PCI.
- Wall Motion Score [ Time Frame: 0-6 months ]The score is measured by simple unit scale (1 = normal, 2 = hypokinetic (muscle impaired), 3= akinetic (muscle dead)). Each of the 16 segments of the hearts is scored, with the total being divided by 16 to derive the score.
- Left ventricular ejection fraction (LVEF) [ Time Frame: 0-6 months ]Left ventricular ejection fraction measurement from echocardiogram will be used to assess cardiac function prior to randomisation, 48 hours and 6 months post primary PCI
- Myocardial Blush Grade [ Time Frame: 0-2 hours ]Myocardial Blush Grade measurement from angiogram will be used to assess cardiac function. The score goes from 0 to 3, with 3 being normal and 0 being absence of myocardial blush
- TIMI Myocardial Perfusion Grade [ Time Frame: 0-2 hours ]Thrombolysis in myocardial infarction score from angiogram will be used to assess myocardial perfusion. This score goes from 0 to 3, 3 indicates normal flow within the artery and 0 indicates a complete coronary occlusion.
- TIMI corrected frame count [ Time Frame: 0-2 hours ]Thrombolysis in myocardial infarction score with corrected frame count from angiogram to assess myocardial perfusion
- Cardiac enzyme measurements [ Time Frame: 0-32 hours ]Cardiac enzyme levels including troponin T, creatine kinase, creatine kinase-MB and high sensitivity troponin T, from blood samples collected during the hospitalisation period (prior to primary PCI and at 8, 16, 24 and 32 hours post primary PCI).
Other Outcome Measures:
- DNA analyses (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for DNA analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- MicroRNA analyses (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for microRNA analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Vasoactive markers (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for vasoactive marker analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Inflammatory markers (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for inflammatory marker analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Angiogenic markers (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for angiogenic marker analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Liver function (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for liver function analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Thyroid Function (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for thyroid function analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Lipid profile (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for lipid profile analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
- Lipoprotein profile (Subject to funding) [ Time Frame: 0-6 months ]Samples of whole blood will be used for lipoprotein profile analyses at baseline, post-PCI, discharge and 6 month follow up (6m follow up for Randomised participants only).
Information from the National Library of Medicine
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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:
- Adult men and women aged over 18 who present with STEMI within 6 hours of symptom onset. Patients will be eligible if they have symptoms consistent with myocardial ischaemia (chest pain, dyspnoea) for at least 20 minutes accompanied by definite ECGs indicating STEMI as defined by Australian National Heart Foundation (NHF) guidelines
- Willing and able to comply with all study requirements, including treatment, assessment and clinic visit attendances
- Able to personally read and understand the Participant Information and Consent Form and provide written, signed and dated informed consent to participate in the study
- (At time of PCI) Patient has received metallic drug-eluting stent
- Participant consents to have a 3-7 day (discharge) and 5 month follow up cardiac MRI
Exclusion Criteria:
At the time of screening and/or prior to randomisation, no known;
- Previous coronary bypass grafting
- Other residual lesions with ≥50% diameter stenosis in the culprit vessel
- Prior myocardial infarction in the target territory
- Presence of contraindications to thrombolytic therapy (including history of stroke and recent brain surgery active internal bleeding; history of cerebrovascular accident; intracranial or intraspinal surgery, or trauma within 2 months; intracranial neoplasm, arteriovenous malformation, or aneurysm; known bleeding diathesis; and severe uncontrolled hypertension)
- Presence of contraindications to adenosine infusion for IMR measurement including sinus node disease, moderate to severe bronchoconstrictive disease and second or third-degree atrioventricular (AV) block
- Diagnosis of metastatic disease
- Concurrent illness, including severe infection that may jeopardise the ability of the patient to undergo the procedures outlined in this protocol with reasonable safety
- Serious medical or psychiatric conditions that might limit the ability of the patient to comply with the protocol
- Pregnancy, lactation, or inadequate contraception. Women must be post-menopausal, infertile, or use a reliable means of contraception. Women of childbearing potential must have a negative pregnancy test done within 7 days prior to registration. Men must have been surgically sterilised or use a (double if required) barrier method of contraception.
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Participation in any investigational study in the previous 30 days
Other exclusion criteria:
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(Dose Finding and Cardiac MRI cohort only) Presence of contraindications to contrast enhanced MRI including severe claustrophobia, pregnancy, pacemakers, non-MRI compatible aneurysm clips, defibrillators and estimated glomerular filtration rate of <30mL/min.
(At time of PCI)
- Patients who received GpIIb/IIIa treatment prior to IMR measurement
- Patients who do not undergo primary PCI due to lack of severity of culprit lesion or other reasons.
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): NCT03998319
Contacts
| Contact: Martin Ng, MBBS (Hons) | +614 3407 8507 | martin.ng@sydney.edu.au | |
| Contact: Rebecca Mister | +612 9562 5000 ext 5342 | RESTORE-MI.Study@sydney.edu.au |
Locations
Show 22 study locations
Sponsors and Collaborators
University of Sydney
Genentech, Inc.
Investigators
| Study Chair: | Martin Ng, MBBS (Hons) | Royal Prince Alfred Hospital, Sydney, Australia | |
| Study Chair: | Andy Yong, MBBS | Concord Repatriation General Hospital | |
| Study Chair: | Anthony Keech, MBBS | National Health and Medical Research Council, Australia | |
| Study Chair: | William Fearon, MD | Stanford University | |
| Study Chair: | Jamie Layland, MBBS | Peninsula Health | |
| Study Chair: | Harvey White, FRCS | Green Lane Cardiovascular Service |
| Responsible Party: | University of Sydney |
| ClinicalTrials.gov Identifier: | NCT03998319 |
| Other Study ID Numbers: |
CTC0150 |
| First Posted: | June 26, 2019 Key Record Dates |
| Last Update Posted: | January 20, 2023 |
| Last Verified: | January 2023 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Plan Description: | Please refer to the NHMRC Clinical Trials Centre publication and data sharing Standard Operating Procedure. |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | Yes |
Keywords provided by University of Sydney:
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STEMI IMR microcirculation microvascular obstruction myocardial infarction |
physiology angioplasty PCI thrombolysis treatment thrombolysis |
Additional relevant MeSH terms:
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ST Elevation Myocardial Infarction Myocardial Infarction Myocardial Ischemia Heart Diseases Cardiovascular Diseases Vascular Diseases Infarction |
Ischemia Pathologic Processes Necrosis Tenecteplase Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action |