A Clinical Investigation of SM-01 Stenting Versus PTA for the Treatment of Superficial Femoral Artery Disease
This study is ongoing, but not recruiting participants.
Sponsor:
Johnson & Johnson K.K. Medical Company
Information provided by:
Johnson & Johnson K.K. Medical Company
ClinicalTrials.gov Identifier:
NCT01183117
First received: August 1, 2010
Last updated: August 17, 2011
Last verified: August 2011
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Purpose
The main objective is to evaluate the safety and efficacy of SM-01 stenting (Cordis S.M.A.R.T.™ Nitinol Stent System) for the treatment of SFA lesions as compared to PTA (balloon angioplasty). If SM-01 is used in a PTA-bailout patient, the case will be assessed separately.
Condition | Intervention | Phase |
---|---|---|
Peripheral Vascular Diseases |
Device: SM-01 Device: PTA |
Phase 3 |
Study Type: | Interventional |
Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
Official Title: | A Clinical Investigation of SM-01 Stenting Versus PTA for the Treatment of Superficial Femoral Artery Disease |
Resource links provided by NLM:
Further study details as provided by Johnson & Johnson K.K. Medical Company:
Primary Outcome Measures:
- Non-TVF(Target-vessel failure) rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]The primary endpoint will be freedom from TVF defined as any events of clinical driven (confirmed by duplex ultrasound or angiography) TLR/TVR, procedure failure, amputation of the target lesion's leg, procedure or device related death, occlusion of target lesion, or > 70% restenosis of target lesion.
Secondary Outcome Measures:
- Procedure Success rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Procedure Success rate for Bailout [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Difference between pre and post proceduer of ABI [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Difference between pre and post procedure of Rutherford Categories [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Non-TLR/TVR rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Primary Patency rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Stent Fracture rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Difference between pre and post procedure of QOL (SF-36) [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
- Major Clinical Event rate [ Time Frame: 12 Months ] [ Designated as safety issue: Yes ]
Estimated Enrollment: | 100 |
Study Start Date: | July 2010 |
Estimated Study Completion Date: | June 2014 |
Estimated Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Experimental: SM-01 |
Device: SM-01
SM-01 is a self-expandable, crush recoverable stent with a diameter larger than that of the arterial lumen. The stent is indicated for use in a vessel with a diameter 1 to 2 mm smaller than the nominal stent diameter. This stent will open to the diameter of the artery and will continue to apply expanding force on the artery.
|
Active Comparator: PTA |
Device: PTA
balloon angioplasty
|
Eligibility
Ages Eligible for Study: | 20 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Age >= 20 years.
- Symptomatic leg ischemia by Rutherford Classification (category1, 2, or 3).
- Lesion length >= 40 mm to <= 150 mm. (must be treatable with no more than two SM-01 stents. Overlap should be about 1cm if two stents are used)
- Reference vessel diameter (RVD) >= 4.0 mm and <= 7.0 mm.
- All lesions are to be located >= 3.0 cm proximal to the superior edge of the patella, and >= 1.0 cm distal to the SFA / PFA bifurcation.
- >= 50% stenosis or total occlusion.
- Patent infrapopliteal and popliteal arteries, i.e., single-vessel runoff or better with at least one of three vessels patent (< 50% stenosis) to the ankle or foot.
- Patient or legally authorized representative must provide written informed consent prior to initiation of study procedures.
- A patient with bilateral obstructive SFA disease is eligible for enrollment into the study. If a patient with bilateral disease is enrolled, the target limb will be the more severe limb. The more severe limb will be selected according to clinical symptomatology. If clinical symptomatology is similar, the more clinically severe lesion will be selected. The contralateral procedure should not be done until at least 30 days after the index procedure of the more severe limb was attempted.
Exclusion Criteria:
- Recent hemorrhagic disease within the past 3 months.
- Aneurysm in the SFA or popliteal artery.
- Acute limb occlusion.
- Procedures which are pre-determined to require stent-in-stent placement to obtain patency, such as severe calcification which is resistant to stenting, or for in-stent restenosis.
- Poor iliac or common femoral "inflow".(However, intervention to restore adequate blood flow prior to the treatment of the study lesion is allowed.)
- Known allergies to aspirin, heparin, or ticlopidine, or bleeding diathesis.
- Patients unable or unwilling to tolerate anticoagulant or antiplatelet therapy.
- Patients unable or unwilling to tolerate contrast agents used in intravascular procedures.
- Allergic to nitinol or tantalum.
- Women who are pregnant or lactating, or of child bearing potential, or with a desire to be a parent during the study period.
- Significant vessel tortuosity or other parameters prohibiting access to the lesion or which would prevent delivery of the stent device.
- Revascularization involving the same limb 30 days prior to the index procedure or a planned re-vascularization within 30 days after the index procedure.
- Previously implanted stent(s) at the same site in the artery to be treated.
- Requiring stent placement in the distal SFA or popliteal artery.
- Presence of a femoral artificial graft.
- History of participating in any other clinical study within 1 year.
- Life expectancy less than 3 years, or any other factors preventing clinical follow-up.
- Receiving dialysis or immunosuppressant therapy
- Serum creatinine level >= 2.0 mg/dL before procedure.
- A principal investigator or a co-principal investigator determines that patient is unsuitable for this study.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01183117
Locations
Japan | |
Toho University Ohashi Medical Center | |
2-17-6, Ohashi, Meguro-ku, Tokyo, Japan |
Sponsors and Collaborators
Johnson & Johnson K.K. Medical Company
Investigators
Principal Investigator: | Takuro Takagi, MD | Toho University Ohashi Medical Center |
More Information
No publications provided
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 17, 2012
No publications provided
Responsible Party: | Serie Kazuo / Director, Johnson and Johnson K.K. Medical Company |
ClinicalTrials.gov Identifier: | NCT01183117 History of Changes |
Other Study ID Numbers: | SM-01 |
Study First Received: | August 1, 2010 |
Last Updated: | August 17, 2011 |
Health Authority: | Japan: Pharmaceuticals and Medical Devices Agency |
Additional relevant MeSH terms:
Vascular Diseases Peripheral Vascular Diseases Peripheral Arterial Disease Cardiovascular Diseases |
Atherosclerosis Arteriosclerosis Arterial Occlusive Diseases |
ClinicalTrials.gov processed this record on October 17, 2012