The ABSORB Bioresorbable Scaffold Below the Knee (BTK) Study

Ischemia Clinical Trial

Official title:

ABSORB BTK Study: A Prospective, Multi-center, Controlled Clinical Evaluation of the Use of a Bioresorbable Drug Eluting Stent (Absorb, Abbott Vascular) in the Arterial Vasculature Below the Knee

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02793349
• Other study ID #: HREC 15/051
• Status: Terminated
• Phase: N/A
• Start date: June 2015
• Est. completion date: June 2017

Study information

• Verified date: April 2019
• Source: The University of New South Wales
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ABSORB BTK Study: A prospective, multicenter, controlled clinical evaluation of the use of a bioresorbable drug eluting stent in the arterial vasculature below the knee

Description:

The aim of this study is to evaluate the performance of a bioresorbable vascular scaffold (BVS) coated with the drug Everolimus. This will be used to treat short length blockages of up to 55mm (5.5cm) in arteries below the knee.

This will be performed to treat patients who have severe leg pain or have developed skin ulcers or gangrene which are not healing due to insufficent blood supply. The ABSORB Everolimus Eluting Bioresorbable Vascular Scaffold works on similar principles of drug eluting stents which have been used for a considerable time in treating blocked arteries. However this product consists of a scaffold coated with a drug so rather than leaving a metallic stent in the blood vessel, this product primarily delivers the drug, gives mechanical support to the blood vessel and once it is no longer needed the scaffold absorbs into the body leaving no permanent metallic implant.

This same device has been used safely and effectively in the arteries which supply the heart both in clinical trials and current practice and has also been evaluated in the leg arteries in a single-centre pilot study. This study aims to evaluate it's use in a larger number of patients in multiple centres and compare that to a historical control group of metal drug eluting stents. The study will evaluate both ultrasound and angiographic derived patency in those arteries out to a 36 month follow-up time point. This data will be collected in patients who fulfill the inclusion criteria and who are then treated and followed over time.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: June 2017
• Est. primary completion date: June 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Stenotic (> 50%) or occlusive atherosclerotic disease of the distal popliteal or infrapopliteal arteries

• A maximum of two focal target lesions in one or more distal popliteal or infrapopliteal vessels

• Length of lesion is maximally 55 mm, allowing maximally 2 stents to be implanted

• Reference vessel diameter should be 2.5 mm-4 mm

• Symptomatic critical limb ischemia (Rutherford 3, 4, 5)

• Subject is able to take at least one type of thienopyridine (e.g. clopidogrel) and acetylsalicylic acid

• The patient must be > 18 years of age

• Life-expectancy of more than 12 months

• The patient has no child bearing potential or negative serum pregnancy test within 7 days of the index procedure

• The patient must be willing and able to return to the appropriate follow-up times for the duration of the study

• The patient must provide written patient informed consent that is approved by the ethics committee

Exclusion Criteria:

• Patient refusing treatment

• The reference segment diameter is not suitable for available stent design.

• Unsuccessfully treated (>30% residual stenosis) proximal inflow limiting arterial stenosis

• Untreatable lesion located at the distal outflow arteries

• More than two infrapopliteal lesions in the same limb

• Previously implanted stent(s) or PTA at the same lesion site

• Lesion location requiring kissing stent procedure

• Lesion lies within or adjacent to an aneurysm

• Inflow-limiting arterial lesions left untreated

• The patient has a known allergy to heparin, Aspirin or other anticoagulant/anti-platelet therapies or a bleeding diatheses or is unable, or unwilling, to tolerate such therapies.

• The patient takes Phenprocoumon (Marcumar).

• The patient has a history of prior life-threatening contrast media reaction.

• The patient is currently enrolled in another investigational device or drug trial.

• The patient is currently breast-feeding, pregnant or intends to become pregnant.

• The patient is mentally ill or retarded.

• Subject has received a heart transplant or any other organ transplant or is on a waiting list for any organ transplant

• Subject is receiving or scheduled to receive anticancer therapy for malignancy within 30 days prior to or after the procedure

• Subject is receiving immunosuppression therapy, or has known serious immunosuppressive disease (e.g., human immunodeficiency virus), or has severe autoimmune disease that requires chronic immunosuppressive therapy (e.g., systemic lupus erythematosus, etc.) The patient should also not receive inhibitors of CYP3A (such as Itraconazole, and Erythromycin), or inducers of CYP3A (Cytochrome P450 3A4) (such as Rifampin) within 90 days following the procedure.

• Subject is receiving or is scheduled to receive chronic anticoagulation therapy (e.g., heparin, coumadin)

• Use of alternative therapy (e.g. atherectomy, cutting balloon, laser, radiation therapy) as part of the index procedure

Related Conditions & MeSH terms

• Arterial Occlusive Diseases
• Ischemia
• Peripheral Arterial Disease
• Peripheral Arterial Disease (PTA
• Peripheral Vascular Diseases

Intervention

Device:
• Absorb Bioresorbable Vascular Scaffold
Absorb Bioresorbable Vascular Scaffold

Locations

Country	Name	City	State
Australia	Epworth Hospital	Melbourne	Victoria
Australia	Prince of Wales Hospital	Sydney	New South Wales
Netherlands	Reinier de Graf Hospital	Delft
New Zealand	Auckland City Hospital	Auckland

Sponsors (1)

Lead Sponsor	Collaborator
The University of New South Wales

Countries where clinical trial is conducted

Australia,  Netherlands,  New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Angiographic patency	Freedom from angiographic binary in-scaffold restenosis (>50% stenosis)	12 months
Secondary	Technical success	Technical success defined as the ability to cross and dilate the lesion to achieve residual angiographic stenosis no greater than 30% and residual stenosis less than 50% by duplex ultrasound (US) imaging.	Procedure
Secondary	Haemodynamic primary, assisted primary and secondary patency	Haemodynamic primary, assisted primary and secondary patency as assessed by ultrasound	1 month
Secondary	Haemodynamic primary, assisted primary and secondary patency	Haemodynamic primary, assisted primary and secondary patency as assessed by ultrasound	6 months
Secondary	Haemodynamic primary, assisted primary and secondary patency	Haemodynamic primary, assisted primary and secondary patency as assessed by ultrasound	12 months
Secondary	Haemodynamic primary, assisted primary and secondary patency	Haemodynamic primary, assisted primary and secondary patency as assessed by ultrasound	24 months
Secondary	Haemodynamic primary, assisted primary and secondary patency	Haemodynamic primary, assisted primary and secondary patency as assessed by ultrasound	36 months
Secondary	Limb salvage rate (LSR)	Limb salvage defined as 1 minus major amputation rate (major amputation is defined as at or above ankle, as opposed to minor amputation being at or below metatarsus preserving functionality of foot)	12 months
Secondary	Target lesion revascularization (TLR)	Target lesion revascularization (TLR) is defined as a repeat intervention to maintain or re-establish patency within the region of the treated arterial vessel plus 5 mm proximal and distal to the treated lesion edge	12 months
Secondary	Rutherford Category	Clinical success defined as an improvement of Rutherford classification of one class or more as compared to the pre-procedure Rutherford classification	12 months
Secondary	Adverse clinical events	Clinical events defined as fatal, life-threatening, or judged to be severe by the investigator; resulted in persistent or significant disability; necessitated surgical or percutaneous intervention; or required prolonged hospitalization	12 months