Skip to main content
OpenTrials
Completed

NCT Number: NCT01415804

Investigation of Stent-grafts in Aortic Dissection (INSTEAD)

The objective of INSTEAD is to compare long-term (5 years) outcomes of endograft prosthesis versus medical management in patients with dissection of the thoracic aorta.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

University Hospital Rostock; Heart Center

Rostock, Mecklenburg-Vorpommern, 18057, Germany

About this study

Patients > 18 years with type B aortic dissection were randomized to either thoracic aortic endoprosthesis (stent-grafting) or antihypertensive management (medical treatment). Only stable patients without spontaneous false lumen thrombosis 14 days after index dissection were considered eligible for study inclusion. Long-term outcome measures included all-cause mortality, aorta-specific mortality and a cluster endpoint (reflecting progression of disease, conversion and additional interventions); the analysis is based on 140 randomized cases followed for at least 5 years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • No contraindication the general anesthesia and ventilation
  • Type B aortic dissection that occurred 2-52 weeks prior to randomization
  • Diameter of the targeted aortic segment < 6 cm
  • Subject or legal guardian understand the nature of teh study and agrees to its provisions on a written informed consent form
  • Availability for appropriate follow-up visits during the F/U period of 5 years
  • Capability to follow all study requirements

Exclusion criteria

  • Pregnancy
  • Thrombocytopenia
  • Ongoing anticoagulation therapy
  • Renal failure and/or creatinine > 2,4 mg%
  • Complete thrombosis of false lumen
  • Cancer likely to cause death within 1 year
  • Enrollment in another clinical study
  • Unwillingness to cooperate with study procedures or F/U visits

Treatment and study plan

endoprosthesis

Device

Thoracic aortic stentgraft

Other names: Talent endoprosthesis

Primary outcomes

  1. All cause mortality

    Time frame: 5 years post randomization

Secondary outcomes

  1. Aorta-specific mortality

    Time frame: 5 years post randomization

  2. Progression of disease

    Time frame: 5 years

  3. Aortic remodeling

    Time frame: 5 years

Sponsors and collaborators

Lead sponsor

University of Rostock

Other

Registry information

Official study title

A Randomized Comparison of Strategies for Type B Aortic Dissection - the INvestigation of STEnt-grafts in Aortic Dissection (INSTEAD) Trial

Acronym: INSTEAD

Important dates

Study start
2002
Primary completion
2010
Study completion
2011
First posted
Aug 12, 2011
Registry last updated
Aug 12, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.