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INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dissection (INSTEAD)

Primary Purpose

Aortic Diseases

Status
Completed
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Medtronic Talent Stent-Graft-System
Sponsored by
Medtronic Bakken Research Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Diseases focused on measuring Aorta, Dissection, Thoracic

Eligibility Criteria

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

Inclusion Criteria:

  • No contraindication for an anesthetic procedure with intubation
  • Type B aortic dissection that occurred 2-52 weeks before randomization
  • Diameter of the targeted aortic segment ≤6 cm
  • Aortic kinking <75°
  • The subject or legal guardian understands the nature of the study and agrees to its provisions on a written informed consent form
  • Availability for the appropriate follow-up visits during the follow-up period
  • Capability to follow all study requirements

Exclusion Criteria:

  • Pregnant woman
  • Thrombocytopenia or ongoing anticoagulation therapy
  • Renal failure and/or creatinine >2.4 mg%
  • Complete thrombosis of the false lumen
  • Ongoing infection
  • Cancer is likely to cause death within 1 year
  • Enrolment in another clinical study
  • Unwillingness to cooperate with study procedures or follow-up visits

Sites / Locations

  • Medtronic Bakken Research Center

Arms of the Study

Arm 1

Arm Type

Active Comparator

Arm Label

1

Arm Description

Anti-hypertensive medical treatment

Outcomes

Primary Outcome Measures

all-cause mortality

Secondary Outcome Measures

thrombosis of the false lumen, cardiovascular morbidity, degree of aortic expansion, length of intensive care and hospital stay, and quantitative assessment of single or combination antihypertensive drug therapy.

Full Information

First Posted
September 4, 2007
Last Updated
October 28, 2015
Sponsor
Medtronic Bakken Research Center
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1. Study Identification

Unique Protocol Identification Number
NCT00525356
Brief Title
INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dissection
Acronym
INSTEAD
Official Title
INvestigation of STEnt Grafts in Patients With Type B Aortic Dissection
Study Type
Interventional

2. Study Status

Record Verification Date
September 2007
Overall Recruitment Status
Completed
Study Start Date
February 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Medtronic Bakken Research Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this study is to compare treatment with an endograft prothesis versus antihypertensive treatment in patients with a dissection of the thoracic aorta.
Detailed Description
Patients older than 18 years with type B aortic dissection as diagnosed by computed tomography or magnetic resonance angiography are randomized to either a thoracic aortic endoprosthesis and antihypertensive treatment, called "stent grafting," or a tailored antihypertensive treatment, called "medical treatment." Only patients in a clinically stable condition and without spontaneous thrombosis of the false lumen after 14 days of the index dissection are considered eligible for study inclusion. Primary outcome measure is all-cause mortality. Secondary outcome variables include conversion to stent and/or surgery, induced thrombosis of the false lumen, cardiovascular morbidity, aortic expansion (>5 mm/y of maximum diameter including true and false lumina), quality of life, and length of intensive care unit and hospital stay. The study design calls for 136 patients to be randomized and monitored for 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Diseases
Keywords
Aorta, Dissection, Thoracic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
136 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Anti-hypertensive medical treatment
Intervention Type
Device
Intervention Name(s)
Medtronic Talent Stent-Graft-System
Other Intervention Name(s)
Endograft
Primary Outcome Measure Information:
Title
all-cause mortality
Time Frame
1 year
Secondary Outcome Measure Information:
Title
thrombosis of the false lumen, cardiovascular morbidity, degree of aortic expansion, length of intensive care and hospital stay, and quantitative assessment of single or combination antihypertensive drug therapy.
Time Frame
5 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: No contraindication for an anesthetic procedure with intubation Type B aortic dissection that occurred 2-52 weeks before randomization Diameter of the targeted aortic segment ≤6 cm Aortic kinking <75° The subject or legal guardian understands the nature of the study and agrees to its provisions on a written informed consent form Availability for the appropriate follow-up visits during the follow-up period Capability to follow all study requirements Exclusion Criteria: Pregnant woman Thrombocytopenia or ongoing anticoagulation therapy Renal failure and/or creatinine >2.4 mg% Complete thrombosis of the false lumen Ongoing infection Cancer is likely to cause death within 1 year Enrolment in another clinical study Unwillingness to cooperate with study procedures or follow-up visits
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
C A Nienaber, MD, FESC, FACC
Organizational Affiliation
Division of Cardiology and Internal Medicine Department, Rostock University, Germany.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medtronic Bakken Research Center
City
Maastricht
ZIP/Postal Code
6229 GW
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
15990739
Citation
Nienaber CA, Zannetti S, Barbieri B, Kische S, Schareck W, Rehders TC; INSTEAD study collaborators. INvestigation of STEnt grafts in patients with type B Aortic Dissection: design of the INSTEAD trial--a prospective, multicenter, European randomized trial. Am Heart J. 2005 Apr;149(4):592-9. doi: 10.1016/j.ahj.2004.05.060.
Results Reference
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PubMed Identifier
19996018
Citation
Nienaber CA, Rousseau H, Eggebrecht H, Kische S, Fattori R, Rehders TC, Kundt G, Scheinert D, Czerny M, Kleinfeldt T, Zipfel B, Labrousse L, Ince H; INSTEAD Trial. Randomized comparison of strategies for type B aortic dissection: the INvestigation of STEnt Grafts in Aortic Dissection (INSTEAD) trial. Circulation. 2009 Dec 22;120(25):2519-28. doi: 10.1161/CIRCULATIONAHA.109.886408. Epub 2009 Dec 7.
Results Reference
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INSTEAD Trial: INvestigation of STEnt Grafts in Patients With Type B Aortic Dissection

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