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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
Deutsches Herzzentrum Muenchen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Vascular Diseases focused on measuring stent, atherectomy, paclitaxel-eluting balloon

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
September 29, 2009
Last Updated
March 6, 2014
Sponsor
Deutsches Herzzentrum Muenchen
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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

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Efficacy Study of Stenting, Paclitaxel Eluting Balloon or Atherectomy to Treat Peripheral Artery Disease

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