The Merit WRAPSODY™ Endovascular Stent Graft for Treatment of Iliac Artery Occlusive Disease

Peripheral Arterial Disease Clinical Trial

Official title:

Prospective Investigation of The Merit WRAPSODY™ Endovascular Stent Graft for Treatment of Iliac Artery Occlusive Disease

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03994185
• Other study ID #: IOD-P2-19-01
• Status: Withdrawn
• Phase: N/A
• Start date: September 2020
• Est. completion date: December 31, 2020

Study information

• Verified date: April 2020
• Source: Merit Medical Systems, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, single-center, non-randomized phase 2, first-in-iliac artery study, to evaluate the safety and effectiveness of the WRAPSODY Stent Graft for the treatment of peripheral arterial occlusive disease in symptomatic subjects with de novo or restenotic lesions in the common iliac artery (CIA) and/or external iliac artery (EIA), including lesions at the aortic bifurcation.

Description:

Approximately 30 subjects will be enrolled. Post study procedure subjects will have planned follow-up visits at 4 weeks, 24, 36 and 52 weeks, and unscheduled visits as medically necessary,

The primary study safety endpoint is the proportion of subjects free from a composite of device- or procedure-related death, myocardial infarction, or amputation above the metatarsals in the treated leg resulting from a vascular event, or device- or procedure-related serious adverse events within 4 weeks of the index procedure. The primary clinical effectiveness endpoint is the proportion of subjects with a composite improvement of at least 1 Rutherford category and patency as evaluated by duplex ultrasound at 4 weeks after index procedure.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 31, 2020
• Est. primary completion date: September 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. Subject has signed informed consent

2. Subject is = 21 years of age

3. Subject is able and willing to comply with study requirements

4. Male, infertile female, or female practicing contraception and a negative pregnancy test within 7 days prior to the study procedure

5. Symptomatic claudication or rest pain without tissue loss, Rutherford category 2-4

6. Angiographic evidence of de novo or restenotic target lesion(s) in native vessels in the common and/or external iliac artery(ies) (multiple stenoses may exist within the target lesion)

7. Total lesion(s) length is = 110mm

8. Target lesion(s) is at least 3 cm from an existing stent or stent graft

9. At least 1 stenosis in the target vessel has = 50% stenosis

10. Target vessel diameter is between 4.6 and 14.4mm at angiographic screening for device placement

11. Adequate ipsilateral blood flow, including at least 1 patent (<50% stenotic) superficial femoral or profundal femoral artery

12. Full expansion of an appropriately sized (in the investigator's opinion) standard angioplasty balloon has been achieved during primary angioplasty at the target lesion prior to enrollment

Exclusion Criteria:

1. Subject has undergone an intervention (surgical or percutaneous) in the target limb(s) <30 days from the date of the index study procedure

2. Subject has a surgical or percutaneous procedure in the target limb(s) planned within 30 days following the index study procedure

3. Previous or planned bypass surgery in the target limb(s)

4. Coronary intervention within 30 days prior to enrollment or planned within 12 months after index study procedure

5. Subject has had a stroke within 90 days prior to the index study procedure

6. Subject has had a transient ischemic attack within 30 days prior to the index study procedure

7. Uncorrectable coagulation disorder

8. Subject cannot receive heparin, dual antiplatelet treatment, or anticoagulant(s) appropriate in the opinion of the investigator

9. Condition unrelated to study anticipated to require indefinite anticoagulation

10. Evidence of blood borne infection

11. Hypersensitivity to nickel titanium alloy

12. Allergy to radiographic contrast material which cannot be adequately premedicated

13. Serum creatinine >2.5mg/dL

14. The subject is enrolled in another investigational study

15. Life expectancy is = 12 months

16. Active malignancy other than non-melanomatous skin cancer

17. Stenosis/restenosis is located within a previously placed stent or stent graft

18. Angiographic evidence of thrombus within or adjacent to the target lesion(s)

19. Aneurysmal dilation proximal or distal to the target lesion(s) that could interfere with placement of the study device

20. Abdominal aortic artery stent, if it could interfere with placement of the study device

21. Target lesion(s) are located such that the stent graft would prevent blood flow to the internal iliac artery, if patent

22. Lesions requiring atherectomy or ablation to facilitate stent graft delivery

23. Any other condition deemed exclusionary in the opinion of the investigator for documented reasons relating to the health and/or welfare of the subject

Related Conditions & MeSH terms

• Iliac Artery Disease
• Iliac Artery Occlusion
• Peripheral Arterial Disease
• Peripheral Vascular Diseases
• Stenosis of Artery

Intervention

Device:
• Placement of WRAPSODY stent graft
Placement of WRAPSODY stent graft into the iliac arteries and/or aortic bifurcation.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Merit Medical Systems, Inc.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety endpoint of subjects free from specified adverse events	The primary study safety endpoint is the proportion of subjects free from a composite of device- or procedure-related death, myocardial infarction, or amputation above the metatarsals in the treated leg resulting from a vascular event, or device- or procedure-related serious adverse events within 4 weeks of the index procedure.	4 weeks after placement of WRAPSODY stent graft
Primary	Effectiveness endpoint of subjects with improvement of Rutherford Category	The primary clinical effectiveness endpoint is the proportion of subjects with improvement of at least 1 Rutherford category within 4 weeks of the index procedure. Composite with Outcome 3.	4 weeks after placement of WRAPSODY stent graft
Primary	Effectiveness endpoint of subjects with patency	The primary clinical effectiveness endpoint is the proportion of subjects with patency as evaluated by duplex ultrasound at 4 weeks after index procedure. Composite with Outcome 2.	4 weeks after placement of WRAPSODY stent graft