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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01354119
Other study ID # ADdistal_graft
Secondary ID
Status Terminated
Phase Phase 4
First received May 13, 2011
Last updated January 13, 2015
Start date January 2011
Est. completion date December 2014

Study information

Verified date January 2015
Source Asan Medical Center
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Background: Aortic stent-graft is useful to occlude intimal tear and prevent further dilatation of the false lumen in patients with aortic dissection. The long-term benefit of aortic stent-graft in patients with uncomplicated distal aortic dissection has not been well demonstrated, especially in patients at high risk of aneurysmal change and death.

Purpose: The purpose of the study is to evaluate long-term clinical benefit of stent-graft insertion performed just after the acute phase into the descending thoracic aorta in patients with distal aortic dissection and at high risk of aneurysmal change of the dissected aorta.


Recruitment information / eligibility

Status Terminated
Enrollment 7
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group N/A to 75 Years
Eligibility Inclusion Criteria:

- Uncomplicated distal aortic dissection

- Initial false lumen diameter >= 22 mm

Exclusion Criteria:

- Old age (> 75 years old)

- Other comorbidity or malignancy with life expectancy < 5 years

- Complicated dissection requiring aortic surgery or intervention

- Sudden death in acute phase

- Marfan syndrome

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Aortic stent-graft
Early intervention with aortic stent-graft

Locations

Country Name City State
Korea, Republic of Asan Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Asan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Aortic aneurysm and death 4 years No
Secondary Events and complications paraplegia cerebrovascular accident aorta surgery 4 years No
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