Coronary Flow Reserve Following Orbital Atherectomy

Abbott

Status: Completed

Conditions: Coronary Artery Disease

Treatments: Device: Coronary Orbital Atherectomy plus Stenting

Study type: Observational

Funder types: Industry

Identifiers

NCT02339545

CLN-0006-P

Details and patient eligibility

About

The purpose of the study was to evaluate coronary artery flow reserve (CFR) following successful percutaneous coronary intervention (PCI) treatment of severely calcified coronary lesions by orbital atherectomy and stenting.

Full description

This is an acute, observational, prospective, multi-center clinical study, evaluating coronary flow reserve (CFR) using the Volcano FloWire®. Subjects will be evaluated after treatment with orbital atherectomy and stenting of de-novo severely calcified lesions, due to coronary artery disease.

Subjects who undergo successful revascularization using the Diamondback 360® Coronary Orbital Atherectomy System (OAS) and stenting are eligible for enrollment. Coronary blood flow of enrolled subjects will be measured with the Volcano FloWire®, Doppler velocity data recorded intra-procedurally, and major adverse cardiac events (MACE) assessed at 24 hours or at discharge, whichever is earlier.

Determination of CFR by Doppler flow measurements can assess physiological changes in the distal vascular bed. The primary endpoint of this study will evaluate coronary flow reserve after successful treatment of severely calcified coronary lesions using OAS and stent deployment. The secondary endpoint will measure the occurrence of post-procedural Major Adverse Cardiac Events (MACE), including cardiac death, acute myocardial infarction (Q wave or non-Q wave), and target vessel revascularization.

Enrollment: 15 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Subjects must meet all inclusion criteria and no exclusion criteria to be eligible to participate in the study.

Inclusion Criteria

1. Subjects must be at least 18 years of age.
2. Subjects must be scheduled for percutaneous coronary intervention involving stent deployment in de novo coronary lesions.
3. The target vessel must be a de-novo coronary artery with a severely calcified lesion.
4. The target vessel reference diameter must be ≥ 2.0mm and ≤ 4.0 mm.
5. The lesion length must not exceed 40 mm.
6. The target vessel must have a thrombolysis in myocardial infarction (TIMI) flow 3 at baseline.
7. The target lesion must have fluoroscopic, intravascular ultrasound (IVUS) or optical coherence tomograph (OCT) evidence of severe calcium deposit at the lesion site based on the protocol definition.
8. The lesion must be crossable with the ViperWire Advance® coronary guide wire.
9. Successful revascularization using OAS and stent deployment as demonstrated by no evidence of stent dissection and no more than 50% stenosis proximal to the stent.

Exclusion Criteria

1. Inability to understand the study or a history of non-compliance with medical advice.

2. Unwilling or unable to sign the informed consent form (ICF).

3. History of any cognitive or mental health status that would interfere with study participation.

4. Currently enrolled in any pre-approval investigational study. Note: This does not apply to long-term post-market studies unless these studies might clinically interfere with the current study endpoints.

5. Female subjects who are pregnant or planning to become pregnant within the study period.

6. Previous myocardial infarction of the target vessel.

7. Known sensitivity to contrast media, which cannot be adequately pre-medicated.

8. Diagnosed with chronic renal failure or has a serum creatinine level > 2.5 mg/dl.

9. History of a stroke or transient ischemic attack (TIA) within six (6) months of the procedure.

10. Active peptic ulcer or upper gastrointestinal (GI) bleeding within six (6) months of the procedure.

11. Wall motion abnormality in the intended vessel target zone.

12. Severe chronic obstructive pulmonary disease (COPD), asthma or current use of the medication: aminophylline.

13. 2nd or 3rd degree atrioventricular (AV) block.

14. Evidence of current left ventricular ejection fraction (LVEF) ≤45% (where current is defined as the latest LVEF measurement completed within the last 6 months).

15. New York Heart Association (NYHA) class III or IV heart failure.

16. Previous coronary artery bypass surgery.

17. Known allergy to atherectomy lubricant components such as soybean oil, egg yolk phospholipids, glycerin and sodium hydroxide.

18. Severe aortic stenosis.

19. Severe left ventricular hypertrophy.

20. Subject with angiographically confirmed evidence of more than 1 lesion requiring intervention.

21. Target vessel has other lesions with greater than 50% diameter stenosis based on visual estimate or on-line quantitative coronary analysis (QCA).

22. Target vessel has angiographically visible or suspected thrombus.

23. Target vessel has a stent from previous PCI unless:

    1. The stent was implanted greater than 30 days prior to the treatment, and
    2. The stent has no higher than 30% in-stent stenosis, and
    3. The stent is on a different branch than the target lesion.

24. Target vessel is excessively tortuous.

25. Target lesion is an ostial location (within 5 mm of ostium) or an unprotected left main lesion.

26. Target lesion is a bifurcation.

27. Target lesion has a ≥ 1.5 mm side branch.

28. Angiographic evidence of a dissection prior to initiation of orbital atherectomy device (OAD).

29. Angiographic evidence of MACE during procedure.

Trial design

15 participants in 1 patient group

All Enrolled Subjects

Description:

All subjects will receive Coronary Flow Reserve (CFR) measurements post successful orbital atherectomy treatment and stenting.

Treatment:

Device: Coronary Orbital Atherectomy plus Stenting