Efficacy Study of Stenting, Paclitaxel Eluting Balloon or Atherectomy to Treat Peripheral Artery Disease (ISAR-STATH)
Primary Purpose
Peripheral Vascular Diseases
Status
Unknown status
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Stenting (Smart Stent)
Stenting after PEB (Smart Stent, Invatec)
Atherectomy (SilverHawk device)
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Vascular Diseases focused on measuring stent, atherectomy, paclitaxel-eluting balloon
Eligibility Criteria
Inclusion Criteria:
- Symptomatic ≥ 70% stenosis of the SFA (Rutherford stage 2-6)
- Written informed consent
Exclusion Criteria:
- Acute ischemia and/or acute thrombosis of the SFA
- Untreated ipsilateral iliac artery stenosis >70%
- Previous stenting of the SFA
- Popliteal stenosis >70%
- Severe renal insufficiency
Sites / Locations
- Deutsches HerzzentrumRecruiting
- I. Medizinische Klinik, Klinikum rechts der IsarRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
Stenting
Stenting after PEB
Atherectomy
Arm Description
Due to randomization one nitinol stent will be implanted after dilation with a conventional balloon.
Due to randomization one nitinol stent will be implanted after dilation with a Paclitaxel eluting balloon.
The third randomization arm is Atherectomy.
Outcomes
Primary Outcome Measures
Percentage diameter stenosis
Secondary Outcome Measures
All-cause mortality
Major adverse peripheral events (MAPE) defined as acute thrombosis of SFA or ipsilateral amputation or revascularization (PTA or bypass surgery)
Time to onset of any of MAPE.
Binary restenosis rate
Percentage diameter stenosis in duplex ultrasound
Change from baseline in functional status and health related quality of life (Walking Impairment Questionaire)
Full Information
NCT ID
NCT00986752
First Posted
September 29, 2009
Last Updated
March 6, 2014
Sponsor
Deutsches Herzzentrum Muenchen
1. Study Identification
Unique Protocol Identification Number
NCT00986752
Brief Title
Efficacy Study of Stenting, Paclitaxel Eluting Balloon or Atherectomy to Treat Peripheral Artery Disease
Acronym
ISAR-STATH
Official Title
Randomized Trial of Stenting After Dilation With or Without Paclitaxel Eluting Balloon or Atherectomy in Patients With Symptomatic Peripheral Artery Disease
Study Type
Interventional
2. Study Status
Record Verification Date
January 2010
Overall Recruitment Status
Unknown status
Study Start Date
July 2009 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
March 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Deutsches Herzzentrum Muenchen
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the study is to evaluate the efficacy of stenting after dilation with or without paclitaxel-eluting balloon or atherectomy in patients with symptomatic peripheral artery disease.
Detailed Description
The superficial femoral artery is a common place for arteriosclerosis in patients symptomatic for lower extremity vascular disease. Advances in percutaneous transluminal angioplasty (PTA) and stenting have provided new options for the treatment of the disease in this arterial segment. Despite the initial technical success rate of more than 95% the late clinical failure remains an important concern.
Restenosis after PTA occurs in 40-60% within one year. Percutaneous removal of the obstructive material through atherectomy may reduce restenosis rate. So far, data in support of excisional atherectomy derive from registries. Another attempt to reduce restenosis is the use of paclitaxel eluting balloons (PEB). First clinical studies suggest that the use of PEBs during percutaneous treatment of femoropopliteal disease is associated with significant reductions in late lumen loss and target-lesion revascularization.
There is no randomized comparison of this three different interventional strategies. Thus the aim of this study is to evaluate the efficacy of these strategies in terms or reduction of diameter stenosis at follow-up angiogram.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Vascular Diseases
Keywords
stent, atherectomy, paclitaxel-eluting balloon
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Stenting
Arm Type
Active Comparator
Arm Description
Due to randomization one nitinol stent will be implanted after dilation with a conventional balloon.
Arm Title
Stenting after PEB
Arm Type
Experimental
Arm Description
Due to randomization one nitinol stent will be implanted after dilation with a Paclitaxel eluting balloon.
Arm Title
Atherectomy
Arm Type
Experimental
Arm Description
The third randomization arm is Atherectomy.
Intervention Type
Device
Intervention Name(s)
Stenting (Smart Stent)
Other Intervention Name(s)
Smart Stent, Cordis, Johnson & Johnson
Intervention Description
Nitinol stent
Intervention Type
Device
Intervention Name(s)
Stenting after PEB (Smart Stent, Invatec)
Other Intervention Name(s)
Invatec, Smart Stent, Cordis, Johnson & Johnson
Intervention Description
Stenting (nitinol stent) after dilation with Paclitaxel-eluting balloon (PEB).
Intervention Type
Procedure
Intervention Name(s)
Atherectomy (SilverHawk device)
Other Intervention Name(s)
SilverHawk device (EV3 Inc)
Intervention Description
Atherectomy
Primary Outcome Measure Information:
Title
Percentage diameter stenosis
Time Frame
6 months
Secondary Outcome Measure Information:
Title
All-cause mortality
Time Frame
6 and 24 months
Title
Major adverse peripheral events (MAPE) defined as acute thrombosis of SFA or ipsilateral amputation or revascularization (PTA or bypass surgery)
Time Frame
6 months
Title
Time to onset of any of MAPE.
Time Frame
3-24 months
Title
Binary restenosis rate
Time Frame
6 months
Title
Percentage diameter stenosis in duplex ultrasound
Time Frame
6 and 24 months
Title
Change from baseline in functional status and health related quality of life (Walking Impairment Questionaire)
Time Frame
3 and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptomatic ≥ 70% stenosis of the SFA (Rutherford stage 2-6)
Written informed consent
Exclusion Criteria:
Acute ischemia and/or acute thrombosis of the SFA
Untreated ipsilateral iliac artery stenosis >70%
Previous stenting of the SFA
Popliteal stenosis >70%
Severe renal insufficiency
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Klaus Tiroch, MD
Phone
+49-89-1218
Ext
1538
Email
tiroch@dhm.mhn.de
First Name & Middle Initial & Last Name or Official Title & Degree
Tarek Ibrahim, MD
Phone
+49 89-1218
Ext
4018
Email
ibrahim@dhm.mhn.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adnan Kastrati, MD
Organizational Affiliation
Deutsches Herzzentrum München
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ilka Ott, MD
Organizational Affiliation
Klinikum rechts der Isar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Deutsches Herzzentrum
City
Muenchen
ZIP/Postal Code
80636
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Massimiliano Fusaro, MD
Phone
+49 89-1218
Ext
4566
Email
fusaro@dhm.mhn.de
First Name & Middle Initial & Last Name & Degree
Tarek Ibrahim, MD
Phone
+49 89-1218
Ext
4016
Email
ibrahim@dhm.mhn.de
First Name & Middle Initial & Last Name & Degree
Massimiliano Fusaro, MD
Facility Name
I. Medizinische Klinik, Klinikum rechts der Isar
City
Muenchen
ZIP/Postal Code
81675
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ilka Ott, MD
Phone
+49-89-4140
Ext
4360
Email
ott@dhm.mhn.de
First Name & Middle Initial & Last Name & Degree
Ilka Ott, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
28424222
Citation
Ott I, Cassese S, Groha P, Steppich B, Hadamitzky M, Ibrahim T, Kufner S, Dewitz K, Hiendlmayer R, Laugwitz KL, Schunkert H, Kastrati A, Fusaro M. Randomized Comparison of Paclitaxel-Eluting Balloon and Stenting Versus Plain Balloon Plus Stenting Versus Directional Atherectomy for Femoral Artery Disease (ISAR-STATH). Circulation. 2017 Jun 6;135(23):2218-2226. doi: 10.1161/CIRCULATIONAHA.116.025329. Epub 2017 Apr 19.
Results Reference
derived
Learn more about this trial
Efficacy Study of Stenting, Paclitaxel Eluting Balloon or Atherectomy to Treat Peripheral Artery Disease
We'll reach out to this number within 24 hrs