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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06075940




Registration number
NCT06075940
Ethics application status
Date submitted
28/09/2023
Date registered
10/10/2023

Titles & IDs
Public title
Evaluation of the MAGNITUDE® Bioresorbable Drug-Eluting Scaffold in the Treatment of Patients With Below the Knee Disease in Australia
Scientific title
Evaluation of the MAGNITUDE® Bioresorbable Drug-Eluting Scaffold (BRS)in the Treatment of Patients With Below the Knee Disease in Australia
Secondary ID [1] 0 0
CP002
Universal Trial Number (UTN)
Trial acronym
MAGNITUDE-BTK
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Critical Limb-Threatening Ischemia 0 0
Critical Limb Ischemia 0 0
Critical Lower Limb Ischemia 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Other cardiovascular diseases
Cardiovascular 0 0 0 0
Diseases of the vasculature and circulation including the lymphatic system

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - MAGNITUDE BRS

Experimental: MAGNITUDE BRS -


Treatment: Devices: MAGNITUDE BRS
Treatment with the MAGNITUDE Scaffold
Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Primary Safety Endpoint: Freedom from MALE+POD (Major Adverse Limb Event + Peri-Operative Death)
Timepoint [1] 0 0
POD at 30 Days and MALE at 6 months
Primary outcome [2] 0 0
Primary Efficacy Endpoint: Composite of Limb Salvage and Primary Patency
Timepoint [2] 0 0
6 months

Eligibility
Key inclusion criteria
7.1.1 General Inclusion Criteria

1. Subject (or their legally authorized representative) has provided written informed consent prior to any study-related procedure, using the form approved by the Human Research Ethics Committee.
2. Subject agrees not to participate in any other investigational device or drug study for a period of at least 12 months following the index procedure.

Note: Questionnaire-based studies, or other studies that are non-invasive and do not require investigational devices or medications are allowed.
3. Subject has symptomatic chronic limb-threatening ischemia, determined as Rutherford categories 4 or 5.
4. Subject is = 18 years and = 90 years of age.
5. Subject agrees to complete all protocol-required follow-up visits, including angiograms.

7.1.2 Angiographic Inclusion Criteria
6. Target lesion(s) in the infrapopliteal vessel(s) of the same limb located in any of the following vessels: tibioperoneal trunk (TPT), anterior tibial artery (ATA), posterior tibial artery (PTA), or peroneal artery.
7. Target lesion(s) must be located in the proximal 2/3 of the native infrapopliteal vessels and at least 10 cm above the tibio-talar joint.
8. Up to two (2) target lesions and two different arteries can be treated, where all target lesions must be successfully crossed with a guidewire prior to randomization.

Note: For CTO, retrograde crossing of the lesion is allowed but treatment must be via antegrade.

Note: The most distal lesion should be treated before treating more proximal lesions.
9. Distal tibial and pedal runoff for each target lesion must be patent (free of lesions with < 50% stenosis). If the index vessel is either anterior or posterior tibial artery, outflow must be contiguous with a patent dorsalis pedis or common plantar artery.
10. Inflow above-the-knee lesions must be treated successfully (< 30% diameter residual stenosis by angiography without evidence of distal embolization, thrombus formation, or vessel rupture). Presence of hemodynamically significant lesions (>50% stenosis) in the P3 segment of the popliteal artery (infrageniculate) is an exclusion criterion.

Note: Inflow lesions may be treated during the index procedure prior to target lesion(s) using the standard of care (including drug-eluting devices), without wiring the target lesion, if possible. Treatment of inflow lesions in the target limb within prior 30 days is also allowed provided the treatment was successful.

Note: Atherectomy of non-target lesions is not allowed.
11. Target lesion must have reference vessel diameter is between 3.0 - 3.5 mm by angiography. Vessel size measured by IVUS is highly recommended to verify RVD.
12. Target lesion(s) is de novo or restenosed = 70% stenosed by angiography. Note: In-stent restenosis is an exclusion criterion.
13. The total target lesion length among all target lesions must not exceed 11 cm.
14. Minimum target lesion length must be >14 mm.
15. Total scaffold length must not exceed 12 cm, and include at least 2 mm of normal vessel from each pre-dilatation border.
16. The target vessel must not have any other angiographic significant non-target lesions (= 50%).
17. Tandem non-contiguous target lesions are allowed if there is a plaque-free zone of = 2 cm between the lesions. Total lesion lengths must not exceed 11 cm.
18. Target lesion(s) stenting does not block access to patent main named branches (tibioperoneal trunk (TPT), anterior tibial artery (ATA), posterior tibial artery (PTA), or peroneal artery).
19. Non-target below-the-knee lesions in non-target vessels must be successfully treated per standard of care prior to randomization without evidence of thrombosis, distal embolization, or vessel rupture.

Note: Drug-eluting and atherectomy devices for treatment of non-target lesions is not allowed.
20. Subject has suitable common femoral (contralateral or antegrade ipsilateral) vascular access.

Note: Retrograde pedal approach is allowed for crossing but not for treatment of target lesion(s).
21. At least one fully patent below-the-ankle artery (i.e., dorsalis pedis; common with either, lateral, or medial plantar arteries) without hemodynamically significant lesions (= 50% diameter stenosis by angiography) must be present in the target limb.

7.2
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Exclusion Criteria 7.2.1 General Exclusion Criteria

Subjects must not meet any of the following general and angiographic exclusion criteria:

1. Subject with Body Mass Index (BMI) < 18.
2. Subject is pregnant or nursing. Subjects who plan pregnancy during the clinical investigation follow-up period may not be enrolled.

Note: Subjects of child-bearing potential must have a negative pregnancy test = 28 days prior to the index procedure and agree to use contraception for 6 months.
3. Estimated life expectancy <1 year, in the opinion of the Investigator at the time of enrollment.
4. Subject is permanently bedridden.
5. Subject has known hypersensitivity or contraindication to device materials and their degradants (sirolimus, poly (L-lactide), poly (D, L-lactide), lactic acid, or platinum-iridium) or to study medications (including antiplatelet medications) or to contrast media and who cannot be adequately premedicated.
6. Subject has planned surgery or procedure necessitating discontinuation of antiplatelet medications within 6 months after the index procedure.
7. Subject has had revascularization procedure within the target vessel in the previous 3 months
8. Subject has prior major amputation involving the target limb. Note: Major amputation of the contralateral limb is allowed.
9. Subject has planned surgical or endovascular procedure within 6 months following the index procedure.

Note: A planned minor amputation (toe and/or transmetatarsal amputation in either limb) is allowed. Treatment of inflow lesions in the target limb within prior 30 days is also allowed provided the treatment was successful (< 30% residual stenosis, no thrombi, distal emboli or vessel rupture).
10. Subject who has severe ischemia (ABI = 0.39).
11. Subject who has neuropathic lesion(s) with no ischemic component (wounds or ulcers occur on pressure zones of the foot with or without Type 2 diabetes , deformed foot/toes, hematoma, edema ).
12. Subject has presence of osteomyelitis or any gangrene above the metatarsal-phalangeal joints, extensive tissue loss with exposed tendons or requiring complex or recurrent surgeries, full thickness heel ulcer, or pure neuropathic ulcers.
13. Subject with uncontrolled diabetes with HbA1c > 10%.
14. Subject has a prior stroke or myocardial infarction within 3 months of the index procedure.
15. Subject has acute renal failure, severe or end-stage chronic kidney disease (eGFR < 30 mL/min) or requires dialysis.
16. Subject has active systemic infection.
17. Subject is receiving immunosuppression therapy and/or has known immunosuppressive or autoimmune disease (e.g., human immunodeficiency virus, systemic lupus erythematosus, rheumatoid arthritis, severe asthma requiring immunosuppressive medication, etc.).
18. Subject has active malignancy (receiving or scheduled to receive anticancer therapy for malignancy within 1 year prior to or after the index procedure), active blood dyscrasia or coagulation disorder (platelet count < 100,000 cells/mm3 or > 700,000 cells/mm3, a WBC < 3,000 cells/mm3, or hemoglobin < 8.0 g/dl).
19. Subject is an incapacitated individual, defined as a person who is mentally ill, mentally handicapped, or an individual without legal authority to control their activities.
20. Subject has significant comorbid condition(s), or other medical, social, or psychological conditions (such as history of substance abuse, e.g., alcohol, cocaine, heroin, etc.), that in the Investigator's opinion may limit the subject's ability to participate or comply with study instructions and follow-up. This includes subjects with symptomatic COVID-19 infection in the past 2 months or asymptomatic COVID-19 positive test in the past 1 month.

7.2.2 Angiographic Exclusion Criteria
21. Angiographic evidence of thromboembolism or atheroembolism in the target or non-target vessel as confirmed by angiography.
22. Non target lesion located in the popliteal P3 (infrageniculate) segment or treated with atherectomy.
23. Presence of aneurysm or acute thrombus in the aorta or lower extremity arteries.
24. Prior below-the-knee bypass in the target limb.
25. Previously stented lesion(s) or the presence of stents in the target vessel.
26. Target vessel(s) have distal hemodynamically significant lesions (= 50% diameter stenosis by angiography) outside of the allowed treatment zone (presence of non-target lesions in the target vessel is an exclusion criterion).
27. Lesions (target or non-target) with severe calcification (per PACSS 4 classification).
28. Unsuccessful treatment of stenosis (= 50% stenosis) of in-flow arteries.
29. Absence of a patent pedal artery. Absence of contiguous dorsalis pedis or common plantar arteries if the target vessels are anterior or posterior tibial arteries, respectively.
30. Target lesion location requires bifurcation treatment with scaffolding of both branches (kissing scaffold is not allowed). In case of presence of disease at a bifurcation, one vessel can be treated as target and the other as non-target.
31. Lesions (target or non-target) in which successful predilatation cannot be achieved.
32. Planned atherectomy treatment of any target or non-target lesion.

Study design
Purpose of the study
Treatment
Allocation to intervention
Not applicable
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
4/03/2024
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
31/12/2030
Actual
Sample size
Target
30
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 0 0
Prince of Wales Hopsital - Randwick
Recruitment postcode(s) [1] 0 0
2031 - Randwick

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
R3 Vascular Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Kristine Orosz
Address 0 0
Country 0 0
Phone 0 0
1 (408) 420-7446
Fax 0 0
Email 0 0
korosz@r3vascular.com
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT06075940