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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02369848




Registration number
NCT02369848
Ethics application status
Date submitted
9/02/2015
Date registered
24/02/2015
Date last updated
18/04/2018

Titles & IDs
Public title
Shockwave Lithoplasty DISRUPT Trial for PAD (DISRUPT PAD 2)
Scientific title
Shockwave Lithoplasty DISRUPT Trial for PAD (DISRUPT PAD 2)
Secondary ID [1] 0 0
TD 0232
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Peripheral Arterial Disease 0 0
Condition category
Condition code
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
Experimental: Lithoplasty Treatment - Shockwave Lithoplasty System

Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Effectiveness Endpoint Defined as Number of Participants withTarget Lesion Patency by Duplex Ultrasound Defined as Freedom From =50% Restenosis
Timepoint [1] 0 0
12 months post-procedure
Primary outcome [2] 0 0
Safety Endpoint Defined as Composite of New-onset Major Adverse Events (MAEs)
Timepoint [2] 0 0
Within 30 days following procedure
Secondary outcome [1] 0 0
Safety Measured by Number of Participants With Freedom From Major Adverse Events (MAEs)
Timepoint [1] 0 0
12 months
Secondary outcome [2] 0 0
Secondary Endpoint of Acute Procedural Success Achieved in Number of Participants
Timepoint [2] 0 0
Day of Procedure
Secondary outcome [3] 0 0
Secondary Patency Measured by Number of Participants With Target Lesion Patency by Duplex Ultrasound Defined as Freedom From =50% Restenosis.
Timepoint [3] 0 0
6 months
Secondary outcome [4] 0 0
Secondary Patency Measured by Number of Participants With Target Lesion Patency (Without Adjunctive PTA) by Duplex Ultrasound Defined as Freedom From =50% Restenosis.
Timepoint [4] 0 0
12 months
Secondary outcome [5] 0 0
Clinical Success - Improvement of Ankle-Brachial Index (ABI) of the Target Limb.
Timepoint [5] 0 0
6 months
Secondary outcome [6] 0 0
Clinical Success - Improvement of Ankle-Brachial (ABI) of the Target Limb.
Timepoint [6] 0 0
12 months
Secondary outcome [7] 0 0
Clinical Success
Timepoint [7] 0 0
6 months
Secondary outcome [8] 0 0
Clinical Success
Timepoint [8] 0 0
12 months
Secondary outcome [9] 0 0
Clinical Success
Timepoint [9] 0 0
30 days

Eligibility
Key inclusion criteria
1. Subject is able and willing to comply with all assessments in the study.
2. Subject or subject's legal representative have been informed of the nature of the study, agrees to participate and has signed the approved consent form.
3. Age of subject is >18.
4. Rutherford Clinical Category 2, 3, or 4.
5. Resting ankle-brachial index (ABI) of =0.90, or =0.75 after exercise, of the target leg.
6. Estimated life expectancy >1 year.

Angiographic

1. Subject is a suitable candidate for angiography and endovascular intervention in the opinion of the investigator or per hospital guideline.
2. Target lesion that is located in a native de novo superficial femoral artery (SFA) or popliteal artery (popliteal artery extends to and ends proximal to the ostium of the anterior tibial artery).
3. Target lesion reference vessel diameter is between 3.50mm and 7.0mm by visual estimate.
4. Target zone is =150mm in length. Target lesion can be all or part of the 150mm zone.
5. Target lesion is =70% stenosis by investigator via visual estimate.
6. Subject has at least one patent tibial vessel on the target leg with runoff to the ankle (not supported by collateral circulation.) Tibial vessel patency is defined as no stenosis >50%.
7. Ability to pass the guidewire across the atherosclerotic lesion.
8. No evidence of aneurysm or acute or chronic thrombus in target vessel.
9. Calcification is at least moderate. (Presence of fluoroscopic evidence of calcification: 1) on parallel sides of the vessel and 2) extending = 50% the length of the lesion.)
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Rutherford Clinical Category 5 and 6.
2. Subject has active infection in the target leg.
3. Planned major amputation of the target leg (transmetatarsal or higher).
4. The use of chronic total occlusion (CTO) re-entry devices.
5. CTOs greater than 80 mm in length.
6. Any in-stent restenosis within the target zone.
7. Lesions within 10 mm of ostium of the SFA.
8. Highly tortuous arteries (bends greater than 30 degrees over the arc length of the balloon).
9. Target lesion within native or synthetic vessel grafts.
10. History of prior endovascular or surgical procedure on the index limb within the past 30 days.
11. Subject has significant stenosis (>50% stenosis) or occlusion of inflow tract before target treatment zone (e.g. iliac or common femoral) not successfully treated with Plain old Balloon Angioplasty (POBA) or stent and without complications.
12. Subject requires treatment of a peripheral lesion on the ipsilateral limb distal and beyond the 150mm target zone at the time of the enrollment/index procedure.
13. Subject has a known coagulopathy or has a bleeding diatheses, thrombocytopenia with platelet count less than 100,000/microliter, or International Normalized Ratio (INR) >1.5.
14. Subject in whom antiplatelet, anticoagulant, or thrombolytic therapy is contraindicated.
15. Subject has known allergy to contrast agents or medications used to perform endovascular intervention that cannot be adequately pre-treated.
16. Subject has known allergy to urethane, nylon, or silicone.
17. Myocardial infarction within 60 days prior to enrollment.
18. History of stroke within 60 days prior to enrollment.
19. History of unstable coronary artery disease or other uncontrollable comorbidity resulting in hospitalization within the last 60 days prior to enrollment.
20. History of thrombolytic therapy within two weeks of enrollment.
21. Subject has acute or chronic renal disease (e.g., as measured by a serum creatinine of >2.5 mg/dL or >220 umol/L), or on dialysis.
22. Subject is pregnant or nursing.
23. Subject is participating in another research study involving an investigational agent (pharmaceutical, biologic, or medical device) that has not reached the primary endpoint.
24. Subject has other medical, social or psychological problems that, in the opinion of the investigator, preclude them from receiving this treatment, and the procedures and evaluations pre- and post-treatment.

Study design
Purpose of the study
Treatment
Allocation to intervention
NA
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
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
Austria
State/province [1] 0 0
Graz
Country [2] 0 0
Austria
State/province [2] 0 0
Vienna
Country [3] 0 0
Germany
State/province [3] 0 0
Bad Krozingen
Country [4] 0 0
Germany
State/province [4] 0 0
Leipzig
Country [5] 0 0
Germany
State/province [5] 0 0
Munster
Country [6] 0 0
Germany
State/province [6] 0 0
Rosenheim
Country [7] 0 0
New Zealand
State/province [7] 0 0
Auckland

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Shockwave Medical, 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
Thomas Zeller, MD
Address 0 0
Universitäts-Herzzentrum Freiburg & Bad Krozingen
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


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.