Evaluation of a Thin Strut Metallic Stent: the Elixir DynamX Clinical Study

Coronary Artery Disease Clinical Trial

Official title:

Evaluation of a Thin Strut Metallic Stent: the Elixir DynamXTM Novolimus Eluting Coronary Bioadaptor System

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03429894
• Other study ID #: ELX-CL-1704
• Status: Completed
• Phase: N/A
• Start date: November 16, 2017
• Est. completion date: December 31, 2021

Study information

• Verified date: July 2022
• Source: Elixir Medical Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The DynamX (Bioadaptor) study is a prospective, consecutive enrollment study designed to enroll up to 50 patients requiring treatment of a single, de novo lesion ≤ 24 mm in length located in a vessel ≥ 2.5 mm and ≤ 3.5 mm in diameter. All patients be followed clinically at 30 days, 6 and 9 months, and 1, 2 and 3 years. All patients will undergo imaging (angiography and IVUS) follow-up with approximately one-half of the patients returning for follow up at 9 months and approximately one-half returning for follow up at 12 months.

Description:

The DynamX (Bioadaptor) study is a prospective, consecutive enrollment study designed to enroll up to 50 patients requiring treatment of a single, de novo lesion ≤ 24 mm in length located in a vessel ≥ 2.5 mm and ≤ 3.5 mm in diameter. All patients be followed clinically at 30 days, 6 and 9 months, and 1, 2 and 3 years. All patients will undergo imaging (angiography and IVUS) follow-up with approximately one-half of the patients returning for follow up at 9 months and approximately one-half returning for follow up at 12 months. At select centers, a subset of approximately 20 patients will undergo FFR pressure wire measurement at baseline and at follow-up (or at a minimum follow-up) in conjunction with the IVUS imaging, and will also undergo OCT imaging at 9 or 12 months. The primary safety endpoint is Target Lesion Failure at 6 months. TLF is a composite endpoint defined as cardiac death, target vessel MI, and clinically-indicated target lesion revascularization. The primary imaging/efficacy endpoints for those patients undergoing imaging follow-up is the change in mean in-device area and mean lumen area at 9 or 12 months compared to post-procedure as measured by IVUS. Co-primary imaging/efficacy endpoints for those patients undergoing imaging follow-up is late lumen loss as measured by QCA and IVUS at 9 or 12 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: December 31, 2021
• Est. primary completion date: September 17, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

General Inclusion Criteria:

1. Patient must be at least 18 years of age.

2. Patient is able to verbally confirm understanding of risks, benefits and treatment alternatives of receiving the DynamX Novolimus Eluting Coronary Stent System (CSS) and he/she provides written informed consent, as approved by the appropriate Ethics Committee of the respective clinical site, prior to any clinical study related procedure.

3. Patient must have evidence of myocardial ischemia (e.g., stable or unstable angina, silent ischemia, positive functional study or electrocardiogram (ECG) changes consistent with ischemia)

4. Patient must be an acceptable candidate for coronary artery bypass graft (CABG) surgery

5. Patient must agree to undergo all clinical study required follow-up visits, angiograms, and IVUS testing

6. Patient must agree not to participate in any other clinical study for a period of one year following the index procedure. Angiographic Inclusion Criteria - Target Lesion/Vessel

1. Target lesion must be located in a native coronary artery with a nominal vessel diameter of = 2.5 and =3.5 mm assessed visually or by online QCA

2. Target lesion must measure = 24 mm in length

3. Target lesion must be in a major artery or branch with a visually estimated stenosis of = 50% and < 90% with a TIMI flow of = 2

4. The lesion must be successfully pre-dilated (less than 35% DS) prior to enrollment Angiographic Inclusion Criteria - non-Target Lesion/Vessel Treatment

1. Treatment of a single, non-target lesion located in a separate major epicardial vessel (defined as LAD with septal and diagonal branches, LCX with obtuse marginal and/or ramus intermedius branches and RCA and any of its branches) attempted during the index procedure must be completed first using an approved 'olimus drug eluting stent. The segment must be located such that any injury that might occur during intervention can be clearly attributable to the treated non-target vessel. If the procedure is deemed uncomplicated and optimal, treatment of the target lesion with the DynamX stent can be considered.

Optimal lesion/vessel treatment defined as:

• < 10% but no more than 15% residual diameter stenosis by visual assessment
• no evidence of dissection
• no evidence of thrombus in the treated lesion or vessel
• TIMI 3 flow
• Stent completely covers lesion and extends to healthy vessel on both sides (healthy to healthy) General Exclusion Criteria

1. Patient has a known diagnosis of acute myocardial infarction (AMI) within 72 hours preceding the index procedure and CK and CK-MB have not returned within normal limits at the time of procedure

2. Patient is currently experiencing clinical symptoms consistent with AMI

3. Patient requires the use of any rotablator intervention during the index procedure

4. Patient has current unstable arrhythmias

5. Patient presenting with heart failure, chronic arrhythmia, COPD or lung function impairment

6. Patient has a known left ventricular ejection fraction (LVEF) < 30%

7. Patient has received a heart transplant or any other organ transplant or is on a waiting list for any organ transplant

8. Patient is receiving or scheduled to receive chemotherapy for malignancy within 30 days prior to or after the procedure

9. Patient is receiving immunosuppression therapy and has known immunosuppressive or autoimmune disease (e.g. human immunodeficiency virus, systemic lupus erythematosus etc.)

10. Patient is receiving chronic anticoagulation therapy (e.g., heparin, coumadin) that cannot be stopped and restarted according to local hospital standard procedures.

11. Patient has a known hypersensitivity or contraindication to aspirin, both heparin and bivalirudin, clopidogrel, prasugrel or ticagrelor, Novolimus, CoCr alloys, PLLA polymers or contrast sensitivity that cannot be adequately pre-medicated

12. Elective surgery is planned within the first 6 months after the procedure that will require discontinuing either aspirin or clopidogrel or other P2Y12 inhibitors.

13. Patient has a platelet count < 100,000 cells/mm3 or > 700,000 cells/mm3, a WBC of < 3,000 cells/mm3, or documented or suspected liver disease.

14. Patient has known renal insufficiency (e.g., serum creatinine level of more than 2.5 mg/dL, or patient on dialysis)

15. Patient has a history of bleeding diathesis or coagulopathy or will refuse blood transfusions

16. Patient has had a cerebrovascular accident (CVA) or transient ischemic neurological attack (TIA) within the past six months

17. Patient has had a significant GI or urinary bleed within the past six months

18. Patient has extensive peripheral vascular disease that precludes safe 6 French sheath insertion

19. Patient has other medical illness (e.g., cancer or congestive heart failure) or known history of substance abuse (alcohol, cocaine, heroin etc.) that may cause non-compliance with the clinical study plan, confound the data interpretation or is associated with a limited life expectancy (i.e., less than one year)

20. Patient is already participating in another clinical study which has not reached the primary endpoint (long-term follow-up is not an exclusion)

21. Women of childbearing potential who have not undergone surgical sterilization or are not post-menopausal (defined as amenorrheic for at least one year) as well as women who are pregnant or nursing

22. Patient is unable to give their consent, is legally incompetent, or is institutionalized by virtue of an order issued by the courts or other authority Angiographic Exclusion Criteria

1. Target lesion(s) meets any of the following criteria:

1. Aorto-ostial location

2. Left main location

3. Tapering within target segment of 0.5mm or greater

4. Located within 10 mm of the origin of the LAD or LCX

5. Located within an arterial or saphenous vein graft or distal to a diseased arterial or saphenous vein graft

6. Lesion involving a side branch >2mm in diameter or bifurcation

7. Previous placement of a stent proximal to or within 10 mm of the target lesion

8. Total or sub-total occlusion (TIMI flow = 1)

9. Excessive tortuosity or angulation (= 45o) proximal to or within the lesion

10. The proximal target vessel or target lesion is moderately or severely calcified by visual assessment, or lesion prevents full pre-dilatation balloon expansion

11. Previous intervention restenosis

2. The target vessel contains visible thrombus

3. Another clinically significant lesion (>40%) is located in the same major epicardial vessel as the target lesion (including side branches)

4. Patient has a high probability that a procedure other than pre-dilatation and stenting and (if necessary) post-dilatation will be required at the time of index procedure for treatment of the target vessel (e.g. atherectomy, cutting balloon)

5. Target vessel was previously treated with any type of PCI < 6 months prior to index procedure

6. Non-Target vessel was previously treated with any type of PCI < 30 days prior to the index procedure

Related Conditions & MeSH terms

• Coronary Artery Disease

Intervention

Device:
• Percutaneous Coronary Intervention
Drug eluting stent implant

Locations

Country	Name	City	State
Belgium	AZ Middelheim Hospital	Antwerp
Italy	Ospendale San Raffaele	Milan

Sponsors (1)

Lead Sponsor	Collaborator
Elixir Medical Corporation

Countries where clinical trial is conducted

Belgium,  Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Acute Recoil	Acute Recoil by QCA	During Procedure
Other	Minimum Lumen Diameter (MLD)	MLD by QCA	During Procedure
Other	% Diameter Stenosis (DS)	% DS by QCA	During Procedure
Other	Late Lumen Loss (LLL)	Late lumen loss (in-stent and in-segment) by QCA	9 months
Other	Change in mean and minimum lumen, stent and vessel areas from post-procedure	Change in mean lumen are, device area and vessel area by IVUS	9 or 12 months
Other	In-stent % neointimal obstruction	In-stent % neointimal obstruction by IVUS	9 or 12 months
Other	In-stent late lumen loss (LLL)	In-stent late lumen loss (LLL) byIVUS	9 or 12 months
Other	Vasomotion (Pulsatility)	Vasomotion (Pulsatility) assessment at during systole and diastole by IVUS	9 or 12 months
Other	Stent malapposition	Acute, persistent and late stent malapposition by IVUS	During procedure, 9 or 12 months
Other	Fractional Flow Reserve (FFR)	FFR measurements in the treated vessel	During procedure, 9 or 12 months
Other	Assessment of disengagement segments	Assessment of disengagement segments by OCT	9 or 12 months
Other	Incomplete scaffold/device apposition	Incomplete scaffold/device apposition by OCT	9 or 12 months
Other	Scaffold/Device Area and Lumen Area	Scaffold/Device Area and Lumen Area on OCT	9 or 12 months
Primary	Target Lesion Failure (TLF)	Target Lesion Failure (composite of cardiac death, target vessel MI, and clinically-indicated target lesion revascularization)	6 months
Primary	Change in Mean In-Device Area compared to post-procedure as measured by IVUS		9 or 12 months
Primary	Change in Mean Lumen Area compared to post-procedure as measured by IVUS		9 or 12 months
Primary	Late Lumen Loss (LLL) as measured by QCA		9 or 12 months
Primary	Late Lumen Loss (LLL) as measured by IVUS		9 or 12 months
Secondary	Device Success	Successful delivery of the device and a final residual stenosis < 30% by QCA	During Procedure
Secondary	Procedure Success	Successful delivery of the device and a final residual stenosis < 30% by QCA without TLF through hospital discharge	In Hospital through Discharge
Secondary	Target Lesion Failure (TLF)	Target Lesion Failure (composite of cardiac death, target vessel MI, and clinically-indicated target lesion revascularization)	30 days, 1, 2 and 3 years
Secondary	Cardiac Death	Cardiac Death	30 days, 180 days, 1, 2 and 3 years
Secondary	Non-Cardiac Death	Non-Cardiac death	30 days, 180 days, 1, 2 and 3 years
Secondary	Q-wave Myocardial Infarction (Q-MI)	Q-MI	30 days, 180 days, 1, 2 and 3 years
Secondary	Non-Q-wave Myocardial Infarction (NQ-MI)	NQ-MI	30 days, 180 days, 1, 2 and 3 years
Secondary	Target Vessel Myocardial Infarction (TV-MI)	Target Vessel MI	30 days, 180 days, 1, 2 and 3 years
Secondary	Non-Target Vessel Myocardial Infarction (NTV-MI)	Non-Target Vessel MI	30 days, 180 days, 1, 2 and 3 years
Secondary	Clinically-Indicated Target Lesion Revascularization (CI-TLR)	CI-TLR	30 days, 180 days, 1, 2 and 3 years
Secondary	Non-Clinically Indicated Target Lesion Revascularization (Non-CI-TLR)	Non-CI-TLR	30 days, 180 days, 1, 2 and 3 years
Secondary	Clinically Indicated Target Vessel Revascularization (CI-TVR)	CI-TVR	30 days, 180 days, 1, 2 and 3 years
Secondary	Non-Clinically Indicated Target Vessel Revascularization	Non-CI-TVR	30 days, 180 days, 1, 2 and 3 years
Secondary	Target Vessel Failure (TVF)	Composite of cardiac death, target vessel MI, clinically indicated target vessel revascularization	30 days, 180 days, 1, 2 and 3 years
Secondary	Stent Thrombosis	Definite & Probable Stent Thrombosis (per ARC)	30 days, 180 days, 1, 2 and 3 years