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Intracoronary Stenting and Angiographic Results: Optimizing Treatment of Drug Eluting Stent In-Stent Restenosis 4 (ISAR-DESIRE 4)

Primary Purpose

Restenosis, Stable Angina Pectoris, Acute Coronary Syndrome

Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Paclitaxel Eluting Balloon + Scoring Balloon
Paclitaxel Eluting Balloon
Sponsored by
Deutsches Herzzentrum Muenchen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Restenosis focused on measuring In-stent Restenosis, Drug Eluting Stent, Paclitaxel Coated Balloon, Scoring Balloon, Cutting Balloon, Angiographic follow-up, Optical coherence tomography (OCT)

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% restenosis after prior implantation of LES in native coronary vessels.
  • Written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
  • In women with childbearing potential a negative pregnancy test is mandatory.

Exclusion Criteria:

  • Age < 18 years
  • Cardiogenic shock
  • Acute ST-elevation myocardial infarction within 48 hours from symptom onset.
  • 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.
  • Severe renal insufficiency (glomerular filtration rate ≤ 30 ml/min)
  • Contraindications to antiplatelet therapy, paclitaxel, stainless steel, cobalt, chrome
  • Therapy including Lovastatin, Ciclosporin, Terfenadine, Midazolam, or Ondansetron
  • Pregnancy (present, suspected or planned) or positive pregnancy test.
  • Previous enrollment in this trial.
  • Patient's inability to fully comply with the study protocol.

Sites / Locations

  • Deutsches Herzzentrum Muenchen
  • 1. Med. Klinik am Klinikum rechts der Isar der TU Muenchen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Paclitaxel Eluting Balloon + Scoring Balloon

Paclitaxel Eluting Balloon

Arm Description

Dilatation of the lesion with an Paclitaxel Eluting Balloon before the utilization of a Scoring Balloon

Paclitaxel Eluting Balloon

Outcomes

Primary Outcome Measures

In-segment percent diameter stenosis
In-segment percent diameter stenosis (%DS) at 6-8 month follow-up angiography

Secondary Outcome Measures

In-stent late lumen loss
The difference between minimal lumen diameter post-procedure and minimal lumen diameter at follow-up angiography
In-segment binary angiographic restenosis
diameter stenosis ≥50% in the in-segment area (including the interventional area as well as 5 mm margins proximal and distal) at follow-up angiography
Death or myocardial infarction
Combined incidence of death or myocardial infarction at one and two year
Target lesion revascularization
Need for target lesion revascularization (TLR), defined as any revascularization procedure involving the target lesion due to luminal re-narrowing in the presence of symptoms or objective signs of ischemia at one and two year follow-up
Target lesion thrombosis
Incidence of target lesion thrombosis at one and two years
OCT tissue characterization
Tissue characterization following application of SCB and PCB using OCT at 6 -8 months follow up

Full Information

First Posted
June 26, 2012
Last Updated
November 18, 2016
Sponsor
Deutsches Herzzentrum Muenchen
Collaborators
Biotronik AG
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1. Study Identification

Unique Protocol Identification Number
NCT01632371
Brief Title
Intracoronary Stenting and Angiographic Results: Optimizing Treatment of Drug Eluting Stent In-Stent Restenosis 4
Acronym
ISAR-DESIRE 4
Official Title
ISAR-DESIRE 4: Randomized Trial Of Scoring Balloon in Patients With Restenosis in "Limus"-Eluting Coronary Stents Undergoing Angioplasty With Paclitaxel-Coated Balloon
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Deutsches Herzzentrum Muenchen
Collaborators
Biotronik AG

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to determine whether scoring balloon (SCB) plus paclitaxel-coated balloon (PCB) is superior to PCB alone for the treatment of restenosis within "limus"-eluting stents (LES)
Detailed Description
The optimal treatment of in-BMS-restenosis seems to be implantation of a DES which is supported by a large body of evidence. Nevertheless, several recent published studies have shown a substantial reduction in late lumen loss and angiographic restenosis using paclitaxel-coated balloons (PCB) for restenotic lesions. Given the increased world-wide use of DES and the use of DES in increasingly complex coronary disease patterns, the number of patients presenting with restenosis after DES implantation will further increase in the coming decade. Data regarding the optimal treatment of in-DES-restenosis are very limited: Implanting a new DES for in-DES-restenosis has been reported to associate with repeat restenosis rates as high as 20%. In addition, an increased risk of stent thrombosis has been associated with complex stenting and with additional DES implantation. Thus, for lesions which develop restenosis after LES implantation, the optimal treatment strategy remains unknown. Few results on small sample-size populations have been reported in patients treated with scoring or cutting balloon (SCB) technology for treatment of BMS restenosis as compared to plain balloon angioplasty. Moreover, the efficacy of SCB angioplasty in DES restenosis has not been adequately addressed. Furthermore, the potential additive benefit of SCB angioplasty in patients undergoing PCB therapy remains to be elucidated. The hypothesis behind this concept is that the application of SCB prior to deployment of PCB may increase the bioavailability of paclitaxel within the restenotic tissue, and therefore may increase the efficacy of PCB. There are numerous preclinical studies to support this hypothesis, which show that lesion preparation is an important pre-requisite for the effectiveness of PCB.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Restenosis, Stable Angina Pectoris, Acute Coronary Syndrome
Keywords
In-stent Restenosis, Drug Eluting Stent, Paclitaxel Coated Balloon, Scoring Balloon, Cutting Balloon, Angiographic follow-up, Optical coherence tomography (OCT)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
252 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Paclitaxel Eluting Balloon + Scoring Balloon
Arm Type
Experimental
Arm Description
Dilatation of the lesion with an Paclitaxel Eluting Balloon before the utilization of a Scoring Balloon
Arm Title
Paclitaxel Eluting Balloon
Arm Type
Active Comparator
Arm Description
Paclitaxel Eluting Balloon
Intervention Type
Device
Intervention Name(s)
Paclitaxel Eluting Balloon + Scoring Balloon
Intervention Description
Scoring/cutting balloon lesion predilation; paclitaxel eluting balloon therapy
Intervention Type
Device
Intervention Name(s)
Paclitaxel Eluting Balloon
Intervention Description
Standard balloon lesion predilation; paclitaxel-eluting balloon therapy
Primary Outcome Measure Information:
Title
In-segment percent diameter stenosis
Description
In-segment percent diameter stenosis (%DS) at 6-8 month follow-up angiography
Time Frame
6-8 months
Secondary Outcome Measure Information:
Title
In-stent late lumen loss
Description
The difference between minimal lumen diameter post-procedure and minimal lumen diameter at follow-up angiography
Time Frame
6-8 months
Title
In-segment binary angiographic restenosis
Description
diameter stenosis ≥50% in the in-segment area (including the interventional area as well as 5 mm margins proximal and distal) at follow-up angiography
Time Frame
6-8 month
Title
Death or myocardial infarction
Description
Combined incidence of death or myocardial infarction at one and two year
Time Frame
1 and 2 years
Title
Target lesion revascularization
Description
Need for target lesion revascularization (TLR), defined as any revascularization procedure involving the target lesion due to luminal re-narrowing in the presence of symptoms or objective signs of ischemia at one and two year follow-up
Time Frame
1 and 2 years
Title
Target lesion thrombosis
Description
Incidence of target lesion thrombosis at one and two years
Time Frame
1 and 2 years
Title
OCT tissue characterization
Description
Tissue characterization following application of SCB and PCB using OCT at 6 -8 months follow up
Time Frame
6-8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% restenosis after prior implantation of LES in native coronary vessels. Written, informed consent by the patient or her/his legally-authorized representative for participation in the study. In women with childbearing potential a negative pregnancy test is mandatory. Exclusion Criteria: Age < 18 years Cardiogenic shock Acute ST-elevation myocardial infarction within 48 hours from symptom onset. 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. Severe renal insufficiency (glomerular filtration rate ≤ 30 ml/min) Contraindications to antiplatelet therapy, paclitaxel, stainless steel, cobalt, chrome Therapy including Lovastatin, Ciclosporin, Terfenadine, Midazolam, or Ondansetron Pregnancy (present, suspected or planned) or positive pregnancy test. Previous enrollment in this trial. Patient's inability to fully comply with the study protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adnan Kastrati, MD
Organizational Affiliation
Deutsches Herzzentrum Munich
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Robert Byrne, MB PhD
Organizational Affiliation
Deutsches Herzzentrum Munich
Official's Role
Principal Investigator
Facility Information:
Facility Name
Deutsches Herzzentrum Muenchen
City
Munich
State/Province
Bavaria
ZIP/Postal Code
80636
Country
Germany
Facility Name
1. Med. Klinik am Klinikum rechts der Isar der TU Muenchen
City
Munich
State/Province
Bavaria
ZIP/Postal Code
81675
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
28683939
Citation
Kufner S, Joner M, Schneider S, Tolg R, Zrenner B, Repp J, Starkmann A, Xhepa E, Ibrahim T, Cassese S, Fusaro M, Ott I, Hengstenberg C, Schunkert H, Abdel-Wahab M, Laugwitz KL, Kastrati A, Byrne RA; ISAR-DESIRE 4 Investigators. Neointimal Modification With Scoring Balloon and Efficacy of Drug-Coated Balloon Therapy in Patients With Restenosis in Drug-Eluting Coronary Stents: A Randomized Controlled Trial. JACC Cardiovasc Interv. 2017 Jul 10;10(13):1332-1340. doi: 10.1016/j.jcin.2017.04.024.
Results Reference
derived

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Intracoronary Stenting and Angiographic Results: Optimizing Treatment of Drug Eluting Stent In-Stent Restenosis 4

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