Intravascular Balloon Lithotripsy in Left Main Stem Percutaneous Coronary Intervention
Study Details
Study Description
Brief Summary
The IVL Left Main study is a prospective non-randomised pilot study to investigate the mechanical and procedural outcomes and safety of distal left main stenting with coronary lithotripsy in addition to standard techniques in patients with calcific left main disease and a clinical indication for revascularisation.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: PCI to left main with IVL
|
Device: Left main stenting with intravascular lithotripsy
Intravascular lithotripsy (IVL) will be used to modify coronary artery calcification prior to stent implantation in left main coronary disease. Intravascular ultrasound (IVUS) will be used pre and post IVL and post stenting.
|
Outcome Measures
Primary Outcome Measures
- Primary effectiveness endpoint 1 [Time of procedure]
Mean MSA (mm2) by segment for segments with obstructive disease and ≥ 270 degrees calcification.
- Primary effectiveness endpoint 2 [Time of procedure]
Incidence of residual area stenosis <50% by segment for segments with obstructive disease and ≥ 270 degrees calcification.
- Primary safety endpoint [30 days]
Incidence of Major Adverse Cardiac Events (MACE) at 30 days MACE consists of cardiac death, myocardial infarction and target vessel revascularisation
Secondary Outcome Measures
- Minimum stent diameter (MSD) (mm) for segments with obstructive disease and ≥ 270 degrees calcification [Time of procedure]
- Stent symmetry ratio for segments with obstructive disease and ≥ 270 degrees calcification [Time of procedure]
- Stent expansion index (%) for segments with obstructive disease and ≥ 270 degrees calcification [Time of procedure]
- MSA (mm2) for all segments. [Time of procedure]
- MSD (mm) for all segments. [Time of procedure]
- Stent symmetry ratio for all segments. [Time of procedure]
- Stent expansion (%) for all segments. [Time of procedure]
- Device crossing success [Time of procedure]
ARC-2 criteria
- Angiographic success [Time of procedure]
ARC-2 criteria
- Procedural success [Time of procedure]
ARC-2 criteria
- Serious angiographic complications [24-48 hours]
ARC-2 criteria. Composite of loss of major vessel/side branch, embolisation, disruption of collateral flow, persistent slow-flow or no reflow, major dissection, new regional wall motion abnormality, imaging evidence of loss of viable myocardium.
- MACE at 12 months [12 months]
- Individual components of MACE at 30 days [30 days]
- Individual components of MACE at 12 months [12 months]
- Canadian Cardiovascular Society (CCS) angina status at 30 days [30 days]
- Canadian Cardiovascular Society (CCS) angina status at 12 months [12 months]
- Stroke at 30 days [30 days]
- Stroke at 12 months [12 months]
- Target lesion failure (TLF) at 30 days [30 days]
- Target lesion failure (TLF) at 12 months [12 months]
- Target vessel failure (TVF) at 30 days [30 days]
- Target vessel failure (TVF) at 12 months [12 months]
- All-cause mortality [12 months]
Stratified by i) cardiac death ii) non-cardiac death
- Peri-procedural myocardial infarction [48 hours]
ARC-2 criteria
- Spontaneous myocardial infarction [12 months]
ARC-2 criteria
- Ischaemic-driven revascularisation [12 months]
- All revascularisation [12 months]
- Angiographic and intracoronary imaging predictors of mechanical and procedural outcomes [12 months]
- Correlation between CK-MB and/or troponin levels post-PCI and outcomes at 30-days and 12 months [12 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Subject is ≥ 18 years old.
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Unprotected distal LM (or equivalent) disease defined as:
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70% diameter stenosis (DS) on angiography in the distal LM; or
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≥50% DS in the distal LM with a) non-invasive evidence of ischaemia referable to a hemodynamically significant left main lesion, and/or b) FFR ≤0.80; or
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70% diameter stenosis in either the ostial left anterior descending (LAD) or ostial left circumflex (LCX) that is within 10 mm of the ostium and requires stenting back into the LM (distal LM equivalent); or
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50% diameter stenosis in either the ostial left anterior descending (LAD) or ostial left circumflex (LCX) that is within 10 mm of the ostium and requires stenting back into the LM (distal LM equivalent) with a) non-invasive evidence of ischaemia referable to its myocardial territory and/or b) FFR ≤0.80
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Clinical indication for revascularisation by PCI
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Viability of the treatment vessel as determined by echocardiography, cardiac MRI or other equivalent imaging modality.
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≥ 270° arc of calcification within at least one stenotic segment demonstrated on intravascular imaging.
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Ability to pass a 0.014" guide wire across the lesion.
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Ability to provide informed consent and comply with all study procedures, including follow-up at 30 days.
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Lesions not related to the distal LM requiring PCI can be treated:
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at the time of the study procedure if completed prior to distal LM PCI and the procedure was successful and uncomplicated (defined as a final lesion angiographic diameter stenosis <30% and TIMI 3 flow (visually assessed) for all non-target lesions and vessels without perforation, cardiac arrest or need for defibrillation or cardioversion or hypotension/heart failure requiring mechanical or intravenous hemodynamic support or intubation. In situations where the distal LM lesion is critical, the LM can be ballooned or treated first so long as the study protocol is not deviated.
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as a staged procedure either within the same hospital admission or within 30 days. Any staged procedure must be declared at the index procedure otherwise it will be recorded as an event.
Exclusion Criteria:
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Subject is participating in another research study involving an investigational agent (pharmaceutical, biologic, or medical device) that has not reached the primary endpoint.
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Daughter vessel reference diameter < 2.5 mm.
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Use of rotational atherectomy, scoring or cutting balloon, or any investigational device.
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Evidence of aneurysm in target vessel within 10 mm of the target lesion.
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Prior PCI of the LM or PCI of the proximal LAD or proximal LCX within 10 mm of the ostium.
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Prior coronary artery by-pass graft (CABG) surgery.
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Chronic total occlusion (CTO) of the LM, proximal LAD or proximal LCX.
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Untreated pre-procedural haemoglobin < 8 g/dL.
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Renal failure with serum creatinine > 2.5 mg/dL and not on chronic dialysis.
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Uncontrolled diabetes defined as a HbA1c >10%.
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Coagulopathy manifested by platelet count < 50,000/ mL or International Normalized ratio (INR) > 1.7 (INR is only required in patients who have taken warfarin within 2 weeks of enrolment).
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Cardiogenic shock.
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Ongoing ST elevation myocardial infarction (STEMI).
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History of stroke or transient ischemic attack (TIA) within 3 months.
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NYHA class IV heart failure or LVEF < 20%.
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Active peptic ulcer or upper gastrointestinal (GI) bleeding within 6 months.
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Patients with a life expectancy of less than 1 year.
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Visible thrombus (by angiography) at target lesion site.
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Patient has active systemic infection on the day of the index procedure with either fever or requiring intravenous antibiotics.
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Patient has vascular connective tissue disease (e.g. Marfan's syndrome).
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Patient has a hypercoagulable disorder.
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Patient has allergy to imaging contrast media for which they cannot be pre-medicated.
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Allergy to Aspirin.
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Allergy to Clopidogrel, Ticagrelor and Prasugrel.
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Allergy to any component of the drug eluting stent that is planned for use.
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Patient has any other severe comorbidity that is felt to preclude enrolment by the investigator.
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Subject is pregnant or nursing (a negative pregnancy test is required for women of child-bearing potential within 7 days prior to enrolment).
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Belfast Health & Social Care Trust | Belfast | Northern Ireland | United Kingdom | |
| 2 | Golden Jubilee Hospital | Clydebank | Scotland | United Kingdom | |
| 3 | University Hospitals Bristol NHS Foundation Trust | Bristol | United Kingdom | ||
| 4 | King's College Hospital NHS Foundation Trust | London | United Kingdom | ||
| 5 | Royal Brompton & Harefield NHS Foundation Trust | London | United Kingdom | ||
| 6 | St George's University Hospitals NHS Foundation Trust | London | United Kingdom |
Sponsors and Collaborators
- St George's, University of London
- St George's University Hospitals NHS Foundation Trust
- Shockwave Medical, Inc.
Investigators
- Principal Investigator: James Spratt, St George's University Hospitals NHS Foundation Trust
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2019.0329