Utility, Safety, and Effectiveness of the Bard LifeStent 5F Vascular Stent System

Peripheral Arterial Disease Clinical Trial

— REALITY III  

Official title:

A Prospective Study of the Performance of the Bard LifeStent 5F Vascular Stent System

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03071146
• Other study ID #: BPV-16-004
• Status: Completed
• Start date: February 15, 2017
• Est. completion date: May 31, 2018

Study information

• Verified date: August 2018
• Source: C. R. Bard
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The medical device being examined in this study is the Bard® LifeStent® 5F Vascular Stent System. It is intended for use in patients who suffer from peripheral artery disease (PAD). PAD is generally associated with blocked arteries of the legs. The superficial femoral artery (SFA) and popliteal artery are common locations for this problem to develop. The patient may experience pain or discomfort in the leg that occurs when walking or have other complications associated with wound healing. The purpose of this study is to collect information to assess the deliverability, clinical utility, safety and effectiveness of the Bard® LifeStent® 5F Vascular Stent System.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: May 31, 2018
• Est. primary completion date: May 4, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• The subject or legal representative has been informed of the nature of the evaluation, agrees to its provisions, and has signed the informed consent form (ICF).

• Subject agrees to comply with the protocol-mandated follow-up procedures and visits.

• The subject is = 21 years of age.

• The subject has lifestyle-limiting claudication to mild tissue loss defined as:

Rutherford Category 2-5 (moderate claudication to minor tissue loss).

• The target lesion(s) has angiographic evidence of a hemodynamically relevant stenosis or restenosis =50% or occlusion of the SFA and/or popliteal artery (by visual estimate) and is amenable to PTA and stenting.

• The target vessel reference diameter will be (by visual estimate) appropriate for treatment with available stent diameters of 5.0, 6.0 and 7.0 mm.

• A total of two stents may be used to treat a target lesion. Overlapping is allowed.

• There is angiographic evidence of at least one vessel runoff to the foot (at the level of the malleolus).

Exclusion Criteria:

• The subject is unable or unwilling to provide informed consent or is unable or unwilling to comply with the study follow-up procedure and visits.

• The subject has claudication or critical limb ischemia described as Rutherford Category 0 (asymptomatic), 1 (mild claudication), or 6 (major tissue loss).

• The subject has a known contraindication (including allergic reaction) or sensitivity to nickel, titanium or tantalum.

• The subject has a known allergy of hypersensitivity to contrast media which cannot be adequately pre-medicated.

• The subject has a known uncontrolled blood coagulation/bleeding disorder.

• The subject has concomitant renal failure with a creatinine of >2.5 mg/dL.

• The subject has concomitant hepatic insufficiency, thrombophlebitis, uremia, systemic lupus erythematosus (SLE), or deep vein thrombosis (DVT) at the time of the study procedure.

• The subject is receiving dialysis or immunosuppressive therapy.

• The subject is diagnosed with septicemia at the time of the study procedure.

• The subject is participating in an investigational drug or another investigational device study.

• The subject has another medical condition, which, in the opinion of the investigator, may cause him/her to be noncompliant with the protocol, confound the data interpretation, or is associated with limited life expectancy not sufficient to complete all study procedures.

• The subject has extensive peripheral vascular disease, which, in the opinion of the investigator, precludes safe insertion of an introducer sheath.

• The target lesion is located within an aneurysm or associated with an aneurysm in the vessel segment either proximal or distal to the target lesion.

• The subject has angiographic evidence of poor inflow, which would be deemed inadequate to support a vascular bypass graft.

• The subject has severe calcification of the target lesion, which prevents inflation of a PTA balloon (pre-dilatation of the target lesion is required).

• The subject has angiographic evidence of large acute thrombus at the target lesion.

• Subjects with a stent previously implanted into the target lesion. A target vessel with a previously placed stent is permitted as long as the subject device(s) will not come into contact with the previously placed stent during treatment of the target lesion.

• Lesion requiring the use of more than two stents.

• Bilateral disease in the native SFA and/or popliteal artery where both limbs meet the inclusion/exclusion criteria and it is planned to treat both limbs within 30 days. Note: One limb may be enrolled in the study, but only if the second limb is planned to be treated after the 30 day follow-up telephone screening has taken place. The limb that may be enrolled has to be the limb with the more severe lesion and the reasons for treating this specific limb will need to be stated in the case report form (CRF).

• The subject had a prior vascular intervention within 30 days before, or has an intervention planned for within 30 days after the index procedure. Note: Additional non-target lesions may be treated during the index procedure.

Related Conditions & MeSH terms

• Intermittent Claudication
• Peripheral Arterial Disease
• Peripheral Vascular Diseases

Intervention

Device:
• Bard® LifeStent® 5F Vascular Stent System
The LifeStent® Vascular Stent is a peripheral stent intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 240 mm in length in the native superficial femoral artery (SFA) and popliteal artery with reference vessel diameters ranging from 4.0 - 6.5 mm.

Locations

Country	Name	City	State
Germany	Universitaets-Herzzentrum Freiburg, Klinik fuer Kardiologie und Angiologie II	Bad Krozingen	Suedring 15
Germany	Gemeinschaftspraxis fuer Radiologie	Berlin	Heinz-Galinski-Str. 1
Germany	Fuerst-Stirum-Klinik Bruchsal	Bruchsal	Gutleutstr. 1-14
Germany	Praxis fuer Interventionelle Angiologie	Kaiserslautern	Strassburger Allee 4

Sponsors (1)

Lead Sponsor	Collaborator
C. R. Bard

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Freedom from occurrence of death		30 days post-index procedure
Primary	Freedom from occurrence of amputation		30 days post-index procedure
Primary	Freedom from TLR (Target Lesion Revascularization)	TLR is defined as a revascularization procedure (e.g. PTA, cryoplasty, etc.) of the target lesion.	30 days post-index procedure
Primary	Freedom from TVR (Target Vessel Revascularization)	TVR is defined as a revascularization procedure (e.g. PTA, stenting, surgical bypass, etc.) of the target vessel outside the target lesion.	30 days post-index procedure
Primary	Technical success	Technical success is defined as successful deployment and placement accuracy based upon a rating scale completed by the investigators. bookend sizes will be evaluated for clinical utility of size range.	At the time of index procedure (usually within 10 minutes)
Secondary	Freedom from TLR (Target Lesion Revascularization)	TLR is defined as a revascularization procedure (e.g. PTA, cryoplasty, etc.) of the target lesion.	Up to 12 months post-index procedure
Secondary	Freedom from TVR (Target Vessel Revascularization)	TVR is defined as a revascularization procedure (e.g. PTA, stenting, surgical bypass, etc.) of the target vessel outside the target lesion.	Up to 12 months post-index procedure
Secondary	Primary patency rates	Patency is defined as a reduction in luminal diameter (stenosis) of <=50% and of <=70% measured by Duplex ultrasound (DUS) (peak systolic velocity ratio or PSVR <= 2.4 and <=3.4). Failure of primary patency is defined as a restenosis (reduction in luminal diameter of >50%) as measured by DUS (PSVR >2.4).	Up to 12 months post-index procedure
Secondary	Freedom from death	TLR is defined as a revascularization procedure (e.g. PTA, cryoplasty, etc.) of the target lesion. TVR is defined as a revascularization procedure (e.g. PTA, stenting, surgical bypass, etc.) of the target vessel outside the target lesion.	12 months post-index procedure
Secondary	Freedom from occurrence of stroke		12 months post-index procedure
Secondary	Freedom from occurrence of MI (myocardial infarction)		12 months post-index procedure
Secondary	Occurrence of emergent surgical revascularization of the target limb		12 months post-index procedure
Secondary	Occurrence of significant distal embolization in target limb		12 months post-index procedure
Secondary	Occurrence of target limb major amputation		12 months post-index procedure
Secondary	Occurrence of thrombosis of target vessel		12 months post-index procedure.