Safety and Efficacy of the QBX Peripheral Balloon Expandable Stent System in Peripheral Artery Disease (PAD)
- Conditions
- Peripheral Arterial Disease
- Interventions
- Device: QBX (5F/6F) Peripheral Balloon Expandable Stent System
- Registration Number
- NCT05799131
- Lead Sponsor
- QualiMed Innovative Medizinprodukte GmbH
- Brief Summary
This study aims to evaluate the safety and performance of the QBX stent system in the treatment of PAD by reporting of peri- and postoperative complications, including major adverse vascular events (MAVE), Vascular Access Site Complications (VASCs) and bleeding at puncture site, and by evaluating the prevalence of Target Vessel Revascularization (TVR), amputations, procedural success, device performance, reduction in percentage diameter stenosis post-procedure compared to pre-procedure, artery patency, return to normal activity, Rutherford and Fontaine classification, quality of life (QoL), Ankle Brachial Index (ABI), and hospital- and patient-related costs in a prospectively maintained database.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 100
- Patient eligible for implantation of a peripheral balloon-expandable stent.
- Target lesion is an occlusion or diameter stenosis is ≥50% by visual estimate.
- Target lesion is a de novo or restenotic lesion.
- Target lesion is located in the external iliac artery (EIA), internal iliac artery (IIA), common iliac artery (CIA), superficial femoral artery (SFA) and/or deep femoral artery (DFA). Bilateral treatment of the target lesions is allowed. There are no restrictions on the number of target lesions treated with QBX or the number of stents used. Kissing stents and overlapping stents are allowed to treat the target lesions.
- Patient suffers from mild to intermittent claudication (Rutherford 1-3) or critical limb ischemia (Rutherford 4-5).
- Patients with TASC A, B, C and D lesions.
- Patient ≥ 18 years of age at study entry.
- Patient and investigator signed and dated the informed consent form prior to the index-procedure.
- Age < 18 y.
- Pregnant women, women who are currently breastfeeding, women of childbearing potential who are not using an effective method of contraception, or women planning to become pregnant during the course of the study.
- Patients with Rutherford 0 and 6.
- Patient received a different stent device than the study device for the target lesion.
- Target lesion cannot be crossed with a guidewire (e.g. heavily calcified or excessively tortuous target lesion).
- Reference vessel diameter is not suitable for the available stent design.
- Target lesion was previously treated with a stent.
- Target lesion is in a prosthetic vascular bypass graft or within 1 cm of a graft anastomosis.
- Presence of significant stenosis (≥50%) or occlusion of inflow tract not successfully treated before or during the index-procedure (success is measured as < 30% residual stenosis and absence of distal embolization).
- Outflow: In case of treatment of iliac arteries: Inadequate distal runoff with > 50% stenosis of either the common femoral artery or both the superficial and deep femoral arteries. In case of treatment of the SFA: Absence of at least one patent runoff vessel with ≤ 50% stenosis throughout its course (i.e., confirmed in-line patency to the level of the foot). Outflow can be treated before or during the index-procedure (success is measured as < 30% residual stenosis and absence of distal embolization).
- Presence of active inflammation at the planned access site.
- Use of alternative therapy (e.g. atherectomy, cutting balloon, laser, radiation therapy) as part of the index-procedure.
- Patients in severe renal failure (estimated Glomerular filtration rate (eGFR) < 25 mL/min/1.73m). Lab results are maximum 30 days old.
- Patient has a persistent acute intraluminal thrombus of the target lesion.
- Target lesion is in an aneurysm or associated with an aneurysm in the vessel segment either proximal or distal to the target lesion.
- Patient has an abdominal aortic aneurysm contiguous with an iliac artery target lesion.
- Patient suffers from acute limb ischemia defined as any sudden decrease in limb perfusion causing a potential threat to limb viability.
- Contraindication for anti-coagulation therapy (coagulopathy, etc.).
- Patient has a known intolerance to contrast agents. If hypersensitivity to contrast agents in patients with prior reactions could be improved by premedication and changing the contrast agent, the patient can be included in the study.
- Patients has a known hypersensitivity to the stent material (L605).
- Patient has a life expectancy of <12 months.
- Patient has a planned surgical intervention/procedure, interfering with the study (results), within 30 days of the study procedure.
- Patient is considered to be hemodynamically unstable at onset of index-procedure.
- Patient is currently participating in a confounding study.
- Patient is unable to comply with the protocol or proposed follow-up visits.
- Patient is unable / unwilling to provide informed consent.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description QBX (5F/6F) Peripheral Balloon Expandable Stent System QBX (5F/6F) Peripheral Balloon Expandable Stent System -
- Primary Outcome Measures
Name Time Method To evaluate the cumulative rate of MAVE. 12-months follow-up MAVE is defined as:
1. Device- or procedure-related death;
2. Target Lesion Revascularization (TLR) at 12 months, defined as a repeated procedure (endovascular or open surgery) due to a problem arising from the lesion (+1 cm proximally and distally to include edge phenomena) initially treated;
3. Device-related distal embolization that required hospitalization and/or subsequent intervention.
- Secondary Outcome Measures
Name Time Method Intra-operative complication rate. Index-procedure Amputation rate 12-months follow-up Minor (below the ankle) and major (above the ankle) amputation rate at 12 months will be assessed. Major amputation rates must be reported as below-the-knee and above-the-knee amputations.
Procedural success. Index-procedure Procedural success is defined as a combination of technical success, device success and absence of procedural complications.
Post-operative complication rate. 12-months follow-up Re-occlusion rate. 12-months follow-up Re-occlusion is defined as complete occlusion of the target lesion initially treated.
Secondary sustained clinical improvement at 12 months. 12-months follow-up Secondary sustained clinical improvement is defined as sustained upward shift of at least one category on the Rutherford/Fontaine classification including the need for repeated TLR in surviving patients.
Ankle Brachial Index (ABI) during follow-up as compared to baseline. 12-months follow-up Rate of subjects with Vascular Access Site Complications (VASCs) within the first 24h after the index-procedure 24 hours VASCs are defined as:
* Hematoma/bleeding requiring transfusion
* Arterial/venous occlusion/thrombosis
* Severe vasospasm
* Intimal injury/dissection
* Pseudoaneurysm
* Arteriovenous fistula
* Vascular perforation or rupture
* Arterial embolization distal to treatment site
* Neuropathy
* Retroperitoneal hematomaIntra-operative absence of bleeding at puncture site. Index-procedure Target Vessel Revascularization (TVR) rate. 12-months follow-up TVR is defined as a procedure (endovascular or open surgical) due to a problem arising in the target vessel remote from the target lesion(s) initially treated.
Technical success Index-procedure Technical success is defined as successful vascular access and completion of the endovascular procedure and immediate morphological success with less than 30% residual diameter reduction of the treated lesion on completion angiography.
Reduction in percentage diameter stenosis post-procedure compared to pre-procedure. Index-procedure Assessed via CT angio.
Device success. Index-procedure Device success is defined as exact deployment of the device according to the instructions for use.
Distribution of Fontaine stages during follow-up as compared to baseline. 12-months follow-up The percentage of patients with Fontaine stages I to IV will be determined.
Improvement in disease-related health status, functioning and quality of life at follow-up as compared to baseline. 12-months follow-up This is scored by the Walking Impairment Questionnaire and EQ-5D questionnaire.
Device performance. Index-procedure Scored using the following components and a dedicated Scoring System (1: Very good, 2: Good, 3: Sufficient, Poor: 4):
* Insertion through introducer sheath
* Tracking to target site over guidewire
* Crossability through of the lesion
* Catheter pushability
* Catheter shaft kink resistance
* Stent radiopacity
* Inflation time to Nominal diameter
* Deflation time
* Stent apposition
* General usability of the QBX deviceOccurrence of prolonged hospitalization compared to local standard of care (SOC). Immediately after the procedure When the patient leaves the hospital after the procedure.
Time taken off from work for the procedure 1-month follow-up Consists of:
* Initial sick leave after the surgery
* Additional sick leave
* Leave taken by friends/relatives for patient careArtery patency. 12-months follow-up A duplex ultrasound will be performed to evaluate artery patency. If reliable duplex ultrasound assessment of artery patency is not possible, ABI is a good indication of patency. If ABI is abnormal and the patient is experiencing symptoms, a CT angio or other imaging module might be performed according to standard of care.
Return to normal activity. 1-month follow-up The number of days until return to normal activities will be assessed.
Distribution of Rutherford classes during follow-up as compared to baseline. 12-months follow-up The percentage of patients with Rutherford classes 0 to 6 will be determined.
Primary sustained clinical improvement at 12 months. 12-months follow-up Primary sustained clinical improvement is defined as sustained upward shift of at least one category on the Rutherford/Fontaine classification without the need for repeated TLR in surviving patients.
Trial Locations
- Locations (4)
AZ Groeninge
🇧🇪Kortrijk, West-Vlaanderen, Belgium
Ziekenhuis Oost-Limburg Genk
🇧🇪Genk, Limburg, Belgium
HIS IZZ
🇧🇪Brussels, Belgium
Jessa Ziekenhuis
🇧🇪Hasselt, Limburg, Belgium