BATTLE Trial: Bare Metal Stent Versus Paclitaxel Eluting Stent in the Setting of Primary Stenting of Intermediate Length Femoropopliteal Lesions

Peripheral Arterial Disease Clinical Trial

— BATTLE  

Official title:

BATTLE Trial: Bare Metal Stent Versus Paclitaxel Eluting Stent in the Setting of Primary Stenting of Intermediate Length Femoropopliteal Lesions

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02004951
• Other study ID #: RC13_0290
• Status: Terminated
• Phase: N/A
• Start date: March 25, 2014
• Est. completion date: August 7, 2020

Study information

• Verified date: February 2021
• Source: Nantes University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Over the past years, endovascular interventions have become an important part of treatment in patients with peripheral arterial disease.1 Indication for endovascular repair of femoropopliteal lesions has been considerably enlarged as shown in the TASC classification.1 Enlargement of endovascular therapy indication was based on patient choice for a less invasive technique and evidence based medicine. Consequently, TASC classification of lesions has been modified to reflect increased evidence for endovascular treatment of more extensive femoropopliteal lesions, and indication for endovascular repair has been enlarged to more severe TASC types. In summary, endovascular treatment is indicated for TASC A and B lesions which correspond to femoropopliteal lesions ≤15-cm. To treat these lesions, the interventionalists have at their disposal a huge tool box. Evaluation of these tools is crucial to determine the right treatment strategy to avoid further reinterventions and overcosts.

The objective of the BATTLE trial is to compare a bare metal self expandable nitinol stent (Misago RX) versus a paclitaxel eluting stent (Zilver PTX) in the treatment of above-the-knee intermediate length femoropopliteal lesions.

From hospitals in Europe (France, Switzerland) we will randomly assign patients with symptomatic atherosclerotic femoropopliteal lesions to be treated either by bare metal stent or paclitaxel eluting stent. In total, 186 patients will be randomized (93 per group).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 186
• Est. completion date: August 7, 2020
• Est. primary completion date: August 31, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria

• Patient =18 years

• Patient has a history of symptomatic peripheral arterial disease (Rutherford classification: 2-5)

• Lesion is eligible for treatment with a maximum of 2 stents per lesion (treatment of both legs is not permitted)

• Patient is affiliated to the Social Security or equivalent system

• Patient has been informed of the nature of the study, agrees to its provisions (and only for swiss centers, has signed the informed consent form prior to any study related procedure)

• Patient agrees to undergo all protocol required follow-up examinations and requirements at the investigational site

• Reference vessel diameter 4 to 7-mm determined by CT scan (RVD obtained from averaging 5-mm segments proximal and distal to the lesions)

• Target lesion has a pre-procedure percent diameter stenosis of = 50% DS

• De novo atherosclerotic lesions (stenosis and/or occlusion) of the superficial femoral artery, the proximal popliteal artery (P1), or both. The treatment area in the SFA and popliteal artery extended from 1 cm below the origin of the profunda femoris artery to 3 cm above the proximal margin of the intercondylar fossa of the femur.

• Target lesion (single or multiple) has a maximal total length =14-cm and a minimal length = 2-cm

• At least 1 patent runoff vessel (<50% DS throughout its course). The inflow artery(ies) cannot be treated using a drug eluting stent or drug coated balloon.

Exclusion Criteria

• Asymptomatic lesion

• Restenosis

• No atheromatous disease

• Untreated >50% DS of the inflow tract

• Resting ankle brachial index (ABI) unavailable

• Female of child bearing potential

• Patient has received, or is on the waiting list for a major organ transplant

• Patient has a history of coagulopathy or will refuse blood transfusions

• Patient is receiving or scheduled to receive anticancer therapy for malignancy within 1 year prior to or after the procedure

• Severe concomitant disease with life expectation < one year

• Known allergy to paclitaxel

• Contraindication to Aspirin or Clopidogrel and Ticlopidin (the patient must be able to receive Dual Anti-Platelet Treatment for 2 months after the procedure)

• Patient has an infected wound or osteomyelitis on the ipsilateral extremity or foot.

• Patient has had prior major amputation to the ipsilateral (target) extremity

• Patient is not able to give informed consent (and only for swiss centers)

• Patient is currently participating in an investigational drug or device study that has not completed the primary endpoint or that clinically interferes with the current study endpoints Note: Trials requiring extended follow-up for products that were investigational, but have become commercially available since then, are not considered investigational trials

• Patient has previously had, or requires, bypass surgery, endarterectomy or other vascular surgery on any vessel of the ipsilateral extremity

• In the Investigator's opinion patient has (a) co-morbid condition(s) that could limit the patient's ability to participate in the study, compliance with follow-up requirements or impact the scientific integrity of the study

• Target lesion lies within or adjacent to an aneurysm

• Patient with an allergy to contrast agent

• Patient with a severe allergy to metal

• Surgery or endovascular intervention of the target member within 14 days preceding the BATTLE procedure

Related Conditions & MeSH terms

• Femoropopliteal Lesions
• Peripheral Arterial Disease
• Peripheral Vascular Diseases

Intervention

Device:
• Misago RX

• Zilver PTX

Locations

Country	Name	City	State
France	Clinique d'Antony	Antony
France	CHU de Besançon	Besançon
France	CHU de Bordeaux	Bordeaux
France	Centre Hospitalier Pierre Oudot Bourgoin Jallieu	Bourgoin Jallieu
France	CHU de Clermont Ferrand	Clermont Ferrand
France	AP-HP, Hôpital Henri Mondor	Créteil
France	CHU de Lyon	Lyon
France	CHU Nantes	Nantes
France	Clinique Ollioules	Ollioules
France	CHU de Rennes	Rennes
France	Clinique Pasteur	Toulouse

Sponsors (1)

Lead Sponsor	Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Freedom from in-stent restenosis at 1 year	It was defined by restenosis of >50% and by a peak systolic velocity index >2.4 at the target lesion.	1 year
Secondary	residual diameter stenosis	Technical success defined achievement of a final residual diameter stenosis of <30% on the procedural completion angiogram.	Day 0
Secondary	Primary sustained clinical improvement	sustained upward shift of _1 category of the Rutherford classification for claudicants and by wound healing and rest pain resolution for patients in CLI, without the need for repeated TLR in surviving patients.	1 month, 12 months and 24 months
Secondary	Secondary sustained clinical improvement	primary sustained clinical improvement including the need for repeated TLR.	1 month, 12 months and 24 months
Secondary	Primary patency	patency without any percutaneous or surgical intervention in the treated segment or in the adjacent areas.	1 month, 12 months and 24 months
Secondary	Major adverse events	MACEs including all deaths, major amputation.	1 month, 12 months and 24 months
Secondary	Limb salvage	freedom from major ipsilateral amputations	1 month, 12 months and 24 months
Secondary	Death	Death (all cause)	1 month, 12 months and 24 months
Secondary	Ankle brachial index	Ankle brachial index	1 month, 6 months, 12 months and 24 months
Secondary	Target Extremity Revascularization (TER)	TER is defined as any percutaneous intervention or surgical bypass of any segment of the target extremity. The target extremity is defined as the ipsilateral limb arteries proximal and distal to the target lesion, which includes upstream and downstream branches and excludes the target lesion itself.	1 month, 12 months and 24 months
Secondary	Target lesion revascularization (TLR)	TLR expresses the frequency of the need for repeated procedures (endovascular or surgical) due to a problem arising from the stent (1 cm proximally and distally to include edge phenomena) in surviving patients with preserved limb.	1 month, 12 months and 24 months
Secondary	Stent fracture	Stent fractures were assessed by biplane x-rays	1 month, 12 months and 24 months
Secondary	EQ-5D-3L questionnaire	Quality of life - EQ-5D-3L questionnaire EQ-5D-3L = European Quality of Life 5 Dimensions and 3 Lines Scale from 0 to 100. 0 =Worst imaginable state of health 100= Best imaginable state of health	1 month, 12 months and 24 months
Secondary	Economic analysis objective	Incremental cost-effectiveness ratio (ICER) based on quality of life for CUA and on freedom from in-stent restenosis for CEA	2 years