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A Trial to Evaluate the Safety and Efficacy of the Passeo-18 Lux Drug-coated Balloon of Biotronik in the Treatment of the Femoropopliteal Artery Compared to the Medtronic IN.PACT Admiral Drug-coated Balloon. (BIOPACT-RCT)

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ClinicalTrials.gov Identifier: NCT03884257
Recruitment Status : Not yet recruiting
First Posted : March 21, 2019
Last Update Posted : March 21, 2019
Sponsor:
Information provided by (Responsible Party):
ID3 Medical

Brief Summary:

The BIOPACT RCT tiral investigates the efficacy and safety of stenosis, restenosis or occlusions in the femoropopliteal artery of patients presenting a rutherford classification 2,3 or 4 with a Passeo-18 Lux drug-coated balloon of Biotronik. The Paclitaxel eluting balloons are designed for percutaneous transluminal angioplasties in which the balloon will dilate the artery upon inflation and deliver the paclitaxel locally.

An expected total of 151 patients will be treated with the Passeo-18 Lux and compared to a control group of another 151 patients that will be treated with the IN.PACT Admiral drug-coated balloon of Medtronic. Assignment to the treatment groups will be at random. The study will be conducted in two phases. A first pilot study phase of 120 patients distributed evenly over both treatment groups and a second phase to formally test the non-inferiority hypothesis.

The balloon is coated with Paclitaxel intended to avoid cellular proliferation. The drug is released by means of rapid inflation as to release a high dose in a short amount of time. Patients will be invited for a follow-up visit at 1, 6 and 12 months post-procedure.

The primary efficacy endpoints are defined as follows. Freedom from clinically-driven target lesion revascularization at 12 months. Freedom from device- and procedure-related death through 30 days post-index procedure, major target limb amputation through 12 months post-procedure and clinically-driven target vessel revascularization through 12 months post-index procedure. The secondary endpoints are defined as acute device success, acute procedural success , freedom from all cause of death, major target limb amputation and clinically driven target vessel revascularisation through 30 days post-procedure, sustained clinical improvement, no major adverse events through 6 and 12 months post-procedure, primary patency, target lesion revascularisation, target vessel revascularisation, binary restenosis, major target limb amputation, thrombosis at target lesion, change of walking impairment questionnaire score from baseline, change in target limb rutherford classification or ABI.


Condition or disease Intervention/treatment Phase
Peripheral Arterial Disease Device: Passeo-18 Lux treatment group Device: IN.PACT Admiral treatment group Not Applicable

Detailed Description:

The objective of this clinical investigation is to assess the safety and efficacy of the Passeo-18 Lux DCB for the treatment of stenotic, restenotic or occlusive lesions of the femoropopliteal arteries. Furthermore a non-inferiority hypothesis will be tested with the IN.PACT Admiral DCB as comparator.

The patients will be selected based on the investigator's assessment, evaluation of the underlying disease and the eligibility criteria. The patient's medical condition should be stable, with no underlying medical condition which would prevent them from performing the required testing or from completing the study. Patients should be geographically stable, willing and able to cooperate in this clinical study, and remain available for long term follow-up. The patient is considered enrolled in the study after obtaining the patients informed consent, if there is full compliance with the study eligibility criteria and after successful guidewire passage through the study target lesion.

Prior to the index procedure the following will be collected: an informed consent for data collection, demographics, medical history, medication record, physical examination, clinical category of acute limb ischemia (Rutherford category), the resting ankle-brachial index (ABI), blood sample test (complete blood count, comprehensive metabolic panel and if applicable pregnancy test) and a walking impairment questionnaire.

During the procedure the guidewire will cross the entire study lesion after which the lesion will be assessed through angiography. A pre-dilatation with a standard non-drug-coated balloon will be performed followed by a dilatation of the lesion with either a Passeo-18 Lux (Biotronik) or an IN.PACT Admiral balloon (Medtronic). If dilatation was not successful (>30% stenosis, perforation, occlusive or flow limiting dissection) prolonged inflation should be attempted after which bail-out stenting with a bare nitinol stent is allowed in case of inadequate results.

The regular follow-up is necessary to monitor the condition of the patient and the results of the procedure. The patients will be invited for the following required follow-up visits at 1,6 and 12 months. During these visit the following data will be collected: medication record, physical exam, target limb ABI and Rutherford classification, duplex ultrasound of target vessel, walking impairment questionnaire and possible adverse events.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 302 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: The patients will be assigned at random to one of two treatment groups namely the Passeo-18 Lux or the IN.PACT Admiral treatment group.
Masking: Single (Participant)
Masking Description: a single-blind masking will be implemented. The patient won't know which DCB he/she received.
Primary Purpose: Treatment
Official Title: A Randomized Controlled Non-inferiority Trial to Evaluate the Safety and Efficacy of the Passeo-18 Lux Drug-coated Balloon of Biotronik in the Treatment of Subjects With Stenotic, Restenotic or Occlusive Lesions of the Femoropopliteal Artery Compared to the Medtronic IN.PACT Admiral Drug-coated Balloon
Estimated Study Start Date : June 1, 2019
Estimated Primary Completion Date : June 1, 2021
Estimated Study Completion Date : June 1, 2021

Arm Intervention/treatment
Experimental: Passeo-18 Lux treatment group
These patients will be treated with the Passeo-18 Lux (Biotronik).
Device: Passeo-18 Lux treatment group
Percutaneous endovascular angioplasty with the Passeo-18 lux

Active Comparator: IN.PACT Admiral treatment group
These patients will be treated with the IN.PACT Admiral (Medtronic).
Device: IN.PACT Admiral treatment group
Percutaneous endovascular angioplasty with the IN.PACT Admiral




Primary Outcome Measures :
  1. freedom from clinically-driven target lesion revascularization (CD-TLR) at 12 months post-procedure [ Time Frame: 12 months post-procedure ]
    defined as any reintervention at the target lesion due to the following symptoms: drop of ABI >20% or ABI >0.15 compared to the post-procedure ABI.

  2. Safety composite of death, major amputation, and target vessel revascularization (CD-TVR) [ Time Frame: 12 months post-procedure ]
    composite of (1) freedom from device- and procedure-related death through 30 days post-index procedure, (2) freedom from major target limb amputation (above-the-ankle (ATA)) through 12 months post-procedure and (3) clinically-driven target vessel revascularization (CD-TVR) through 12 months post-index procedure


Secondary Outcome Measures :
  1. acute device success [ Time Frame: Index procedure ]
    defined as successful delivery, balloon inflation, deflation and retrieval of the intact study device without burst below rated burst pressure

  2. acute procedural success [ Time Frame: index procedure ]
    defined as restoration of the target lesion with ≤30% residual stenosis in the final angiogram

  3. freedom from all causes of death, freedom from major target limb amputation and freedom from CD-TVR through 30 days [ Time Frame: 1 month post-procedure ]
    freedom from all cause death, major target limb amputation and CD-TVR through 30 days post-procedure

  4. Sustained clinical improvement [ Time Frame: 6 and 12 months post-procedure ]
    defined as freedom from major target limb amputation, TVR, worsening target limb Rutherford class (compared to baseline) and decrease in target limb ankle brachial index (ABI) or toe brachial index (TBI) ≥0.15 (compared to baseline)

  5. freedom from major adverse events [ Time Frame: 6 and 12 months post-procedure ]
    defined as composite of all-cause death, CD-TVR and major target limb amputation, or thrombosis at the target lesion

  6. primary patency rate [ Time Frame: 6 and 12 months post-procedure ]
    defined as a composite of freedom from clinically-driven target lesion revascularization (CD-TLR) and binary restenosis (restenosis defined as duplex ultrasound (DUS) peak systolic velocity ratio (PSVR) ≥2.4 or ≥50% stenosis as assessed by an independent DUS core lab) through 12 months post-index procedure

  7. freedom from target lesion revascularisation [ Time Frame: 6 and 12 months post-procedure ]
    defined as a reintervention to maintain or restore the patency in the target lesion. TLR is clinically-driven (CD) when the TLR was needed due to symptoms or drop of ankle brachial index (ABI) of ≥20% or >0.15 when compared to post-procedure

  8. freedom from target vessel revascularisation [ Time Frame: 6 and 12 months post-procedure ]
    defined as a reintervention to maintain or restore the patency in the target vessel. TVR is clinically-driven (CD) when the TVR was needed due to symptoms or drop of ankle brachial index (ABI) of ≥20% or >0.15 when compared to post-procedure

  9. freedom from binary restenosis [ Time Frame: 6 and 12 months post-procedure ]
    defined as restenosis confirmed by DUS PSVR ≥2.4 or ≥50% stenosis as assessed by independent angiographic and DUS core labs

  10. freedom from major target limb amputation [ Time Frame: 6 and 12 months post-procedure ]
    defined as an amputation above the ankle in the target limb

  11. freedom from thrombosis at target lesion [ Time Frame: 6 and 12 months post-procedure ]
    freedom from thrombosis at target lesion

  12. change in walking impairment questionnaire score from baseline to 6 and 12 months [ Time Frame: 6 and 12 months post-procedure ]

    change in walking impairment questionnaire (WIQ) score from baseline to 6 and 12 months.

    The WIQ consists of 6 sections each consisting of multiple questions. Each question is scored from 0 to 4 (0 meaning a lot of problems and 4 no problems at all). The scores per section are summed up and recalculated to percentages (100% meaning very good and 0% meaning very bad). All the sections are averaged to give the final WIQ-score.


  13. change in target limb rutherford class from baseline to 6 and 12 months [ Time Frame: 6 and 12 months post-procedure ]
    change in target limb rutherford class from baseline to 6 and 12 months

  14. change in target limb resting ABI or TBI from baseline to 6 and 12 months [ Time Frame: 6 and 12 months post-procedure ]
    change in target limb resting ABI or TBI from baseline to 6 and 12 months

  15. freedom from all causes of death [ Time Frame: 6 and 12 months post-procedure ]
    freedom from all causes of death



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Subject is ≥18 years
  • Subject has Rutherford classification 2, 3 or 4
  • Subject has provided written informed consent and is willing to comply with study follow- up requirements
  • De novo stenotic or occlusive lesion(s) or non-stented restenotic or occlusive lesion(s) occurring >90 days after prior plain old balloon (POBA) angioplasty or >180 days after prior DCB treatment
  • Target lesion is located between the ostium of the SFA and the end of the P1 segment of the popliteal artery
  • Target vessel diameter ≥4mm and ≤7mm
  • Target lesion must be stenotic lesion ≤180mm in length (one long lesion or tandem lesions) by investigator's visual estimate or a total occlusion ≤120mm in length by investigator's visual estimate.

Note: tandem lesions must have a total length of ≤180mm by visual estimate and be separated by ≤30mm

  • Target lesion must have angiographic evidence of ≥70% stenosis by investigator's visual estimation
  • Successful, uncomplicated crossing of the target lesion occurs when the tip of the guide wire is distal to the target lesion without the occurrence of flow-limiting dissection or perforation and is judged by visual inspection to be within the true lumen. Subintimal dissection techniques may be used if re-entry occurs above the knee (ATK) and without the use of re-entry devices
  • Target lesion is located at least 30mm from any stent, if target vessel was previously stented
  • After pre-dilatation, the target lesion is ≤50% residual stenosis, absence of a flow-limiting dissection and treatable with available device matrix
  • A patent inflow artery free from significant stenosis (≥50% stenosis) as confirmed by angiography
  • At least one patent native outflow artery to the ankle or foot, free from significant stenosis (≥50% stenosis) as confirmed by angiography

Exclusion Criteria:

  • Acute limb ischemia
  • Patient underwent an intervention involving the target vessel within the previous 90 days
  • Patient underwent any lower extremity percutaneous treatment in the ipsilateral limb using a paclitaxel-eluting stent or DCB within the previous 90 days
  • Patient underwent a percutaneous transluminal angioplasty (PTA) of the target lesion using a DCB within the previous 180 days
  • Women who are pregnant, breast-feeding or intend to become pregnant
  • Patient has life expectancy of less than 1 year
  • Patient has a known allergy to contrast medium that cannot be adequately pre-medicated
  • Patient is allergic to all antiplatelet treatments
  • Patient is receiving immunosuppressant therapy
  • Patient has platelet count <100.000/mm3 or >700.000/mm3
  • Patient has history of gastrointestinal haemorrhage requiring a transfusion within 3 months prior to the study procedure
  • Patient is diagnosed with coagulopathy that precludes treatment with systemic anticoagulation and/or dual antiplatelet therapy (DAPT)
  • Patient has history of stroke within the past 90 days
  • Patient has history of myocardial infarction within the past 30 days
  • Patient is participating in an investigational drug or medical device study that has not completed primary endpoint(s) evaluation or that clinically interferes with the endpoints from this study, or patient is planning to participate in such study prior to the completion of this study
  • Patient has had any major (e.g. cardiac, peripheral, abdominal) surgical procedure or intervention unrelated to this study within 30 days prior to the index procedure or has planned major surgical procedure or intervention within 30 days of the index procedure
  • An intervention in the contralateral limb, planned within 30 days post-index procedure
  • Patient had previous bypass surgery of the target lesion
  • Patient had previous treatment of the target vessel with thrombolysis or surgery
  • Patient is unwilling or unable to comply with procedures specified in the protocol or has difficulty or inability to return for follow-up visits as specified by the protocol
  • Target lesion involves an aneurysm or is adjacent to an aneurysm (within 5mm)
  • Target lesion requires treatment with alternative therapy such as stenting, laser, atherectomy, cryoplasty, brachytherapy or re-entry devices
  • Significant target vessel tortuosity or other parameters prohibiting access to the target lesion
  • Presence of thrombus in the target vessel
  • Iliac inflow disease requiring treatment, unless the iliac artery disease is successfully treated first during the index procedure. Success is defined as ≤30% residual diameter stenosis without death or major complications
  • Presence of an aortic, iliac or femoral artificial graft

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03884257


Contacts
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Contact: Merel Verschueren, MSc +32 (0)52 25 27 45 ext +32 office@id3medical.com
Contact: Baptiste Oosterlinck, Ir. +32 (0)52 25 27 45 ext +32 baptisteoosterlinck@id3medical.com

Locations
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Austria
Medical University of Graz Not yet recruiting
Graz, Austria, 8036
Contact: Marianne Brodmann, Pr       marianne.brodmann@medunigraz.at   
Contact: Romana Schuh       romana.schuh@medunigraz.at   
Principal Investigator: Marianne Brodmann, Pr         
Hanusch Hospital Not yet recruiting
Vienna, Austria, 1140
Contact: Martin Werner, Dr       martin.werner@wgkk.at   
Contact: Schmid       schmid@viennavascular.at   
Principal Investigator: Martin Werner, Dr         
Belgium
OLV Ziekenhuis Aalst
Aalst, Oost-Vlaanderen, Belgium, 9300
UZA Not yet recruiting
Antwerp, Belgium, 2650
Contact: Jeroen Hendriks, Pr.       jeroen.hendriks@uza.be   
Contact: Mieke Hoppenbrouwers    +32 38 21 41 43    Mieke.hoppenbrouwers@uza.be   
Principal Investigator: Jeroen Hendriks, Pr.         
Imelda Hospital
Bonheiden, Belgium, 2820
A.Z. Sint-Blasius
Dendermonde, Belgium, 9200
Z.O.L.
Genk, Belgium, 3600
R.Z. Heilig Hart
Tienen, Belgium, 3300
France
CHU Bordeaux Not yet recruiting
Bordeaux, Nouvelle-Aquitaine, France, 33300
Contact: Eric Ducasse, Pr       eric.ducasse@chu-bordeaux.fr   
Contact: Olivier Periot       olivier.periot@chu-bordeaux.fr   
Principal Investigator: Eric Ducasse, Pr         
Clinique Pasteur Not yet recruiting
Toulouse, Occitanie, France, 3100
Contact: Antoine Sauguet, MD       asauguet@clinique-pasteur.com   
Contact: Frédéric Petit       fpetit@clinique-pasteur.com   
Principal Investigator: Antoine Sauguet, MD         
CHU Nantes Not yet recruiting
Nantes, Pays De La Loire, France, 44093
Contact: Yann Gouëffic, Pr       yann.goueffic@chu-nantes.fr   
Contact: Swanny Fouchard       Swanny.FOUCHARD@chu-nantes.fr   
Principal Investigator: Yann Gouëffic, Pr         
Clinique Rhône Durance Not yet recruiting
Avignon, Provence-Alpes-Côte d'Azur, France, 84000
Contact: Jerôme Brunet, Dr       jeromebrunet@cardiord.fr   
Contact: Chrystel leperchois       leperchois.jacuey@gmail.com   
Principal Investigator: Jerome Brunet, Dr         
Switzerland
Kantonsspital St. Gallen Not yet recruiting
Saint Gallen, Sankt Gallen, Switzerland, 9000
Contact: Lukas Hechelhammer, Dr.       lukas.hechelhammer@kssg.ch   
Principal Investigator: Lukas Hechelhammer, Dr.         
Centre Hospitalier Universitaire Vaudois Not yet recruiting
Lausanne, Vaud, Switzerland, CH-1011
Contact: Sébastien Déglise, Dr       Sebastien.Deglise@chuv.ch   
Principal Investigator: Sébastien Déglise, Dr         
Kantonsspital Winterthur Not yet recruiting
Winterthur, Zürich, Switzerland, 8400
Contact: Christoph Binkert, Pr       christoph.binkert@ksw.ch   
Principal Investigator: Christoph Binkert, Pr         
Triemlispital Zürich Not yet recruiting
Zürich, Switzerland, 8063
Contact: Levent Kara, Dr.       lukas.hechelhammer@kssg.ch   
Principal Investigator: Levent Kara, Dr         
Sponsors and Collaborators
ID3 Medical
Investigators
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Principal Investigator: Koen Deloose, MD AZ Sint-Blasius

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Responsible Party: ID3 Medical
ClinicalTrials.gov Identifier: NCT03884257     History of Changes
Other Study ID Numbers: BIOPACT-RCT_V1.0_14DEC2018
First Posted: March 21, 2019    Key Record Dates
Last Update Posted: March 21, 2019
Last Verified: March 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Peripheral Arterial Disease
Peripheral Vascular Diseases
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases