IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. PTA

Not Applicable

Completed

• Conditions: Peripheral Arterial Disease; Critical Limb Ischemia
• Interventions: Device: DCB; Device: PTA

• Registration Number: NCT02963649
• Lead Sponsor: Medtronic Endovascular

Brief Summary

To assess the safety and efficacy of the paclitaxel drug-eluting balloon IN.PACT 014 versus conventional percutaneous transluminal angioplasty (PTA) for the treatment of patients with chronic total occlusions in the infrapopliteal arteries.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-11-09
• Study First Submitted QC: 2016-11-10
• Study First Posted: 2016-11-15
• Study Start: 2017-03-02
• Primary Completion: 2019-10-07
• Study Completion: 2023-12-21
• Status Verified: 2024-05
• Last Update Submitted: 2024-06-11
• Last Update Posted: 2024-06-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Age ≥18 years.
2. Subject has been informed of the nature of the study, agrees to participate and has signed an EC approved consent form.
3. Female subjects of childbearing potential have a negative pregnancy test ≤7 days before the procedure and are willing to use a reliable method of birth control for the duration of study participation.
4. Subject has documented chronic Critical Limb Ischemia (CLI) in the target limb prior to the study procedure with Rutherford Clinical Category 4 or 5.
5. Subjects with documented infection grade 0-2 and ischemia grade 2-3 according to WIfi classification.
6. Life expectancy >1 year in the Investigator's opinion.
7. Reference Vessel Diameter (RVD) 2 - 4 mm, and confirmed by DUS assessment.
8. Total occlusions with total lesion length ≥ 40 mm.
9. Lesion must be located in the infrapopliteal arteries and above the ankle joint.
10. Multiple lesions can be treated if located in separate vessels.
11. Presence of documented run-off to the foot.
12. Inflow free from flow-limiting lesion confirmed by angiography.
13. Successful pre-dilatation of the (entire) target lesion.

Exclusion Criteria

1. Subject unwilling or unlikely to comply to the appropriate follow-up times for the duration of the study.
2. Planned index limb amputation above the metatarsal level, or any other planned major surgery within 30 days pre or post-procedure.
3. Lesion and/or occlusions located or extending in the popliteal artery or below the ankle joint space.
4. Significant inflow lesion or occlusion in the ipsilateral iliac, SFA and popliteal arteries left untreated.
5. Failure to obtain ≤ 30% residual stenosis in pre-existing, hemodynamically significant inflow lesions in the ipsilateral iliac, SFA and popliteal artery.
6. Prior stent(s) or bypass surgery within the target vessel(s) (including stents placed within target vessels during the index procedure prior to randomization.
7. Previous DCB procedure in the target vessel within 6 months prior to index procedure.
8. Aneurysm in the target vessel.
9. Angiographic evidence of thrombus within target limb.
10. Pre-dilatation resulted in major (≥ Grade D) flow-limiting dissection or residual stenosis > 30%.
11. Use of alternative therapy e.g. atherectomy, cutting balloon, laser, radiation therapy, stents as part of target vessel treatment.
12. Recent MI or stroke < 30 days prior to the index procedure.
13. Heart failure with Ejection Fraction < 30%.
14. Known or suspected active infection at the time of the index procedure, excluding an infection of a lower extremity wound on the target limb.
15. Subjects with infection grade 3 and ischemia grade 0 and 1 according to the Wifi classification.
16. Subjects with neutrotrophic ulcers, heel pressure ulcers or calcaneal ulcers with a risk of major amputation.
17. Subjects with documented active osteomyelitis, excluding the phalanges, that is beyond cortical involvement of the bone per clinical judgement.
18. Impaired renal function (GFR <20 mL/min) and patients on dialysis.
19. Subject with vasculitis, systemic Lupus Erythematosus or Polymyalgia Rheumatica on active treatment.
20. Patient receiving systemic corticosteroid therapy.
21. Known allergies or sensitivities to heparin, aspirin (ASA), other anticoagulant/anti-platelet therapies which could not be substituted, and/or paclitaxel or an allergy to contrast media that cannot be adequately pre-treated prior to the index procedure.
22. The patient is currently enrolled in another investigational device or drug trial that is interfering with the endpoints of this study.
23. Female subjects who are breastfeeding at the time of enrollment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
drug-eluting balloon IN.PACT 014	DCB	product is indicated for PTA in patients with obstructive disease of peripheral arteries with paclitaxel drug - elution.
Standard angioplasty balloon	PTA	standard PTA balloon

Primary Outcome Measures

Name	Time	Method
Efficacy: Late lumen loss (LLL) at 9 months	9 Months	Late lumen loss (LLL) at 9 months

Secondary Outcome Measures

Name	Time	Method
Mechanically-driven Target Lesion Revascularization (TLR) rate	through 37 days	Mechanically-driven Target Lesion Revascularization (TLR) rate
Major Adverse Event (MAE) rate	through 3, 6, 9, 12, 24, 36, 48 and 60 months	defined as a composite of all-cause mortality, target limb major amputation and clinically-driven target lesion revascularization (CD-TLR)
Composite Safety Endpoint	30 days and 9 Months	A composite of freedom from device- and procedure-related mortality within 30 days, freedom from major target limb amputation and freedom from clinically-driven target lesion revascularization (CD-TLR) within 9 months post-index procedure.
Rate of thrombosis at the target lesion	through 30 days, 3, 6, 9, 12, 24, 36, 48 and 60 months	Rate of thrombosis at the target lesion
Device success	at the time of procedure	is defined as successful drug delivery, balloon inflation, deflation and retrieval of the intact study device without burst below the rated burst pressure (RBP).
Status of wound healing	at 30 days, 3, 6, 9, 12, 24 and 36 months	completely healed - improvement - unchanged - worsened
Target Vessel Revascularization (TVR) rate	through 3, 6, 9, 12, 24, 36, 48 and 60 months	Target Vessel Revascularization (TVR) rate
Clinical success	up to discharge visit	is defined as residual stenosis of ≤ 30% without procedural complications (death, major target limb amputation, thrombosis of the target lesion, or target vessel revascularization (TVR))
Functional flow assessment	at 3, 6, 9, 12, 24 and 36 months	is defined as absence of target lesion occlusion (no flow) assessed by duplex ultrasound
Major Target Limb Amputation rate	through 30 days, 3, 6, 9, 12, 24, 36, 48 and 60 months	Major Target Limb Amputation rate
Target Lesion Revascularization (TLR) rate	through 3, 6, 9, 12, 24, 36, 48 and 60 months	Target Lesion Revascularization (TLR) rate
Clinically-driven Target Vessel Revascularization (CD-TVR) rate	through 3, 6, 9, 12, 24, 36, 48 and 60 months	Clinically-driven Target Vessel Revascularization (CD-TVR) rate
Death of any cause and cardiovascular-related deaths	through 3, 6, 9, 12, 24, 36, 48 and 60 months	Death of any cause and cardiovascular-related deaths
Clinically-driven Target Lesion Revascularization (CD-TLR) rate	through 3, 6, 9, 12, 24, 36, 48 and 60 months	Clinically-driven Target Lesion Revascularization (CD-TLR) rate

Trial Locations

Locations (9)

University Hospital Patras; 🇬🇷 Patras, Greece

ZOL Genk; 🇧🇪 Genk, Limburg, Belgium

AZ Sint Blasius; 🇧🇪 Dendermonde, East-Flanders, Belgium

Hopital Guillaume et Rene Laennec - Centre Hospitalier Universitaire; 🇫🇷 Nantes, France

Universitair Ziekenhuis Gent; 🇧🇪 Gent, Belgium

IRCCS Multimedica; 🇮🇹 Sesto San Giovanni, Lombardy, Italy

Maria Cecilia Hospital; 🇮🇹 Cotignola, Ravenna, Italy

Ospedale San Donato; 🇮🇹 Arezzo, Italy

University Hospital Zurich; 🇨🇭 Zürich, Switzerland