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AngioJET Thrombectomy and STENTing for Treatment of Acute Myocardial Infarction

Primary Purpose

Myocardial Infarction

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
rheolytic thrombectomy with direct stenting
direct stenting
Sponsored by
Boston Scientific Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction focused on measuring coronary thrombectomy, thrombectomy for acute myocardial infarction, C14.280.647.500, C14.907.553.355.500

Eligibility Criteria

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

Inclusion Criteria: Patient age > 18 years ST-segment elevation myocardial infarction Angiographically visible thrombus Presentation within 6 hours of symptom onset for primary percutaneous coronary intervention Patient, or relative or legal guardian,provides written informed consent Patient has no childbearing potential or is not pregnant Exclusion Criteria: Prior administration of thrombolysis for current MI Participation in another Study Major surgery within past 6 weeks History of stroke within 30 days, or any history of hemorrhagic stroke Severe hypertension (systolic BP > 200 mm Hg or diastolic BP > 110 mm Hg) not controlled on antihypertensive therapy Known neutropenia ( <1000 neutrophils per mm3) or known severe thrombocytopenia (< 50,000 platelets per mm3) Known prior history of renal insufficiency Co-morbidities with expected survival < 1 year Patient unwilling to receive blood products

Sites / Locations

  • Careggi Hospital, Division of Cardiology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

thrombectomy before stenting

directing stenting alone

Arm Description

thrombectomy before stenting

directing stenting alone

Outcomes

Primary Outcome Measures

ST-segment resolution at 30 minutes post-PCI, assessed by 12-lead ECG
Infarction size measured by technetium Tc 99m sestamibi imaging at 30 days

Secondary Outcome Measures

Post-procedure- TIMI flow, TIMI myocardial blush, and corrected TIMI frame count
30 days- Technetium Tc 99m sestamibi infarct size, MACE
6 months- MACE
12 months- MACE

Full Information

First Posted
January 10, 2006
Last Updated
October 8, 2014
Sponsor
Boston Scientific Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00275990
Brief Title
AngioJET Thrombectomy and STENTing for Treatment of Acute Myocardial Infarction
Official Title
AngioJET Rheolytic Thrombectomy Before Direct Infarct Artery STENTing in Patients Undergoing Primary PCI for Acute Myocardial Infarction: [JETSTENT] Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
August 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Boston Scientific Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether prompt removal of thrombus (blood clot) from a blocked coronary artery using the AngioJet rheolytic thrombectomy device will result in improved blood flow within the heart and a smaller final infarct size (reduced injury to the heart muscle).
Detailed Description
Occlusive thrombosis triggered by a disrupted or eroded atherosclerotic plaque is the anatomic substrate of most acute myocardial infarctions (AMI). Macro- and microembolization of thrombus during percutaneous coronary intervention (PCI) in AMI is frequent and may result in obstruction of the microvessel network, and decreased efficacy of reperfusion and myocardial salvage. Direct stenting without predilation or postdilation is the most simplistic approach to the problem of embolization, and may decrease embolization and the incidence of the no-reflow phenomenon. Other approaches to the problem of microvessel embolization include percutaneous rheolytic thrombectomy (RT) with the AngioJet catheter before stent implantation. The objectives of the study are: to assess whether RT before direct infarct artery stenting results in improved reperfusion success in patients with acute ST-segment elevation myocardial infarction (STEMI) and angiographically evident thrombus; and to validate a technique for use of the AngioJet RT catheter in the treatment of STEMI. Comparisons: Treatment with AngioJet RT immediately before direct infarct artery stenting versus direct stenting alone, in patients with STEMI and angiographically visible thrombus presenting within 6 hours of symptom onset for primary PCI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
coronary thrombectomy, thrombectomy for acute myocardial infarction, C14.280.647.500, C14.907.553.355.500

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
thrombectomy before stenting
Arm Type
Experimental
Arm Description
thrombectomy before stenting
Arm Title
directing stenting alone
Arm Type
Active Comparator
Arm Description
directing stenting alone
Intervention Type
Device
Intervention Name(s)
rheolytic thrombectomy with direct stenting
Intervention Type
Device
Intervention Name(s)
direct stenting
Primary Outcome Measure Information:
Title
ST-segment resolution at 30 minutes post-PCI, assessed by 12-lead ECG
Time Frame
30 minutes post procedure
Title
Infarction size measured by technetium Tc 99m sestamibi imaging at 30 days
Time Frame
30 days post-procedure
Secondary Outcome Measure Information:
Title
Post-procedure- TIMI flow, TIMI myocardial blush, and corrected TIMI frame count
Time Frame
post-procedure
Title
30 days- Technetium Tc 99m sestamibi infarct size, MACE
Time Frame
30 days post-procedure
Title
6 months- MACE
Time Frame
6 months post-procedure
Title
12 months- MACE
Time Frame
12 months post-procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient age > 18 years ST-segment elevation myocardial infarction Angiographically visible thrombus Presentation within 6 hours of symptom onset for primary percutaneous coronary intervention Patient, or relative or legal guardian,provides written informed consent Patient has no childbearing potential or is not pregnant Exclusion Criteria: Prior administration of thrombolysis for current MI Participation in another Study Major surgery within past 6 weeks History of stroke within 30 days, or any history of hemorrhagic stroke Severe hypertension (systolic BP > 200 mm Hg or diastolic BP > 110 mm Hg) not controlled on antihypertensive therapy Known neutropenia ( <1000 neutrophils per mm3) or known severe thrombocytopenia (< 50,000 platelets per mm3) Known prior history of renal insufficiency Co-morbidities with expected survival < 1 year Patient unwilling to receive blood products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Antoniucci, MD
Organizational Affiliation
Azienda Ospedaliero-Universitaria Careggi, Florence, ITALY
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antonio Colombo, MD
Organizational Affiliation
San Raffaelle Hospital, Milan ITALY
Official's Role
Principal Investigator
Facility Information:
Facility Name
Careggi Hospital, Division of Cardiology
City
Florence
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
15081450
Citation
Antoniucci D, Valenti R, Migliorini A, Parodi G, Memisha G, Santoro GM, Sciagra R. Comparison of rheolytic thrombectomy before direct infarct artery stenting versus direct stenting alone in patients undergoing percutaneous coronary intervention for acute myocardial infarction. Am J Cardiol. 2004 Apr 15;93(8):1033-5. doi: 10.1016/j.amjcard.2004.01.011.
Results Reference
background
PubMed Identifier
20691553
Citation
Migliorini A, Stabile A, Rodriguez AE, Gandolfo C, Rodriguez Granillo AM, Valenti R, Parodi G, Neumann FJ, Colombo A, Antoniucci D; JETSTENT Trial Investigators. Comparison of AngioJet rheolytic thrombectomy before direct infarct artery stenting with direct stenting alone in patients with acute myocardial infarction. The JETSTENT trial. J Am Coll Cardiol. 2010 Oct 12;56(16):1298-306. doi: 10.1016/j.jacc.2010.06.011. Epub 2010 Aug 5.
Results Reference
result

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AngioJET Thrombectomy and STENTing for Treatment of Acute Myocardial Infarction

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