Paclitaxel Eluting Balloon and Conventional Balloon for In-Stent Restenosis of the Superficial Femoral Artery (ISAR-PEBIS)
Primary Purpose
Peripheral Vascular Disease
Status
Unknown status
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
PTA
PTA with PEB
Percutaneous Transluminal Angioplasty (PTA)
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Vascular Disease focused on measuring PTA, paclitaxel, restenosis
Eligibility Criteria
Inclusion Criteria:
- Symptomatic ≥ 70% in-stent restenosis of the AFS, (Rutherford stage 2-6)
- Written, informed consent by the patient or her/his legally-authorized representative for participation in the study
Exclusion Criteria:
- Acute ischemia and/or acute thrombosis of the SFA
- Untreated ipsilateral iliac artery stenosis >70%
- Not at least one vessel run-off
- Popliteal involvement with stenosis >70%
- Severe renal insufficiency (GFR <30 ml/min/m2)
- Malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
- Pregnancy (present, suspected or planned) or positive pregnancy test.
- Previous enrollment in this trial.
- Patient's inability to fully cooperate with the study protocol.
Sites / Locations
- 1. Medizinische Klinik, Klinikum rechts der IsarRecruiting
- Deutsches HerzzentrumRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
conventional PTA
PTA with PEB
Arm Description
In stent restenosis is treated with PTA using a conventional balloon.
In stent restenosis is treated with PTA using a paclitaxel eluting balloon.
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
Full Information
NCT ID
NCT01083394
First Posted
February 26, 2010
Last Updated
March 7, 2014
Sponsor
Deutsches Herzzentrum Muenchen
1. Study Identification
Unique Protocol Identification Number
NCT01083394
Brief Title
Paclitaxel Eluting Balloon and Conventional Balloon for In-Stent Restenosis of the Superficial Femoral Artery
Acronym
ISAR-PEBIS
Official Title
Randomized Trial of Paclitaxel Eluting Balloon or Conventional Balloon for Treatment of In-Stent Restenosis of the Superficial Femoral Artery in Patients With Symptomatic Peripheral Artery Disease (ISAR-PEBIS)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2010
Overall Recruitment Status
Unknown status
Study Start Date
March 2010 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
December 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 aim of this study is to perform a randomized, controlled trial to compare percutaneous transluminal angioplasty using paclitaxel eluting balloon (PEB) or using a conventional balloon for treatment of superficial femoral artery in-stent restenosis.
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. Restenosis after PTA occurs in 40-60% within one year. A novel 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 these treatments in patients with in stent restenosis of the superficial femoral artery. Thus, the aim of this study was to compare the efficacy of PTA with conventional balloon or PEB for in stent restenosis in the SFA in terms of 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 Disease
Keywords
PTA, paclitaxel, restenosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
conventional PTA
Arm Type
Active Comparator
Arm Description
In stent restenosis is treated with PTA using a conventional balloon.
Arm Title
PTA with PEB
Arm Type
Experimental
Arm Description
In stent restenosis is treated with PTA using a paclitaxel eluting balloon.
Intervention Type
Device
Intervention Name(s)
PTA
Other Intervention Name(s)
PACIFIC XTREME, Invatec
Intervention Description
PTA using a conventional balloon
Intervention Type
Device
Intervention Name(s)
PTA with PEB
Other Intervention Name(s)
IN.PACT PACIFIC, Invatec
Intervention Description
PTA using a paclitaxel eluting balloon
Intervention Type
Procedure
Intervention Name(s)
Percutaneous Transluminal Angioplasty (PTA)
Other Intervention Name(s)
PACIFIC XTREME or IN.PACT PACIFIC balloons
Intervention Description
Percutaneous transluminal angioplasty with conventional balloon or paclitaxel-eluting balloon
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
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptomatic ≥ 70% in-stent restenosis of the AFS, (Rutherford stage 2-6)
Written, informed consent by the patient or her/his legally-authorized representative for participation in the study
Exclusion Criteria:
Acute ischemia and/or acute thrombosis of the SFA
Untreated ipsilateral iliac artery stenosis >70%
Not at least one vessel run-off
Popliteal involvement with stenosis >70%
Severe renal insufficiency (GFR <30 ml/min/m2)
Malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
Pregnancy (present, suspected or planned) or positive pregnancy test.
Previous enrollment in this trial.
Patient's inability to fully cooperate with the study protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Julinda Mehilli, MD
Phone
+49 89 12 18
Ext
4582
Email
mehilli@dhm.mhn.de
First Name & Middle Initial & Last Name or Official Title & Degree
Ilka V. Ott, MD
Phone
+49 89 41 40
Ext
4360
Email
ott@dhm.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adnan Kastrati, MD
Organizational Affiliation
Deutsches Herzzentrum Muenchen
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ilka V. Ott, MD
Organizational Affiliation
Klinikum rechts der Isar
Official's Role
Principal Investigator
Facility Information:
Facility Name
1. Medizinische Klinik, Klinikum rechts der Isar
City
Muenchen
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ilka V. Ott, MD
Phone
+49 89 4140
Ext
4360
Email
ott@dhm.mhn.de
First Name & Middle Initial & Last Name & Degree
Ilka V. Ott, MD
Facility Name
Deutsches Herzzentrum
City
Muenchen
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
12. IPD Sharing Statement
Citations:
PubMed Identifier
28743787
Citation
Ott I, Cassese S, Groha P, Steppich B, Voll F, Hadamitzky M, Ibrahim T, Kufner S, Dewitz K, Wittmann T, Kasel AM, Laugwitz KL, Schunkert H, Kastrati A, Fusaro M. ISAR-PEBIS (Paclitaxel-Eluting Balloon Versus Conventional Balloon Angioplasty for In-Stent Restenosis of Superficial Femoral Artery): A Randomized Trial. J Am Heart Assoc. 2017 Jul 25;6(7):e006321. doi: 10.1161/JAHA.117.006321.
Results Reference
derived
Learn more about this trial
Paclitaxel Eluting Balloon and Conventional Balloon for In-Stent Restenosis of the Superficial Femoral Artery
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