Aortic-Stent-Register

Status Completed

Clinical Trial Summary

The aims of the aorta-stent-Registry are:

• participating hospitals (with audit) document all consecutive patients diagnosed with a disease of the distal thoracal aorta that receive one of the following therapies:

Clinical Trial Description

1. Endovascular Aorta-Stent-Graft

2. Surgical operation of the distal thoracal aorta

- Documentation of the indications, the procedural results and the clinical short- and long-term results of the endovascular and chirurgical treatment in day to day hospital routine.

- Documentation of the operational risk (Euroscore)

- Documentation of the technical enforcement of the procedure as well as the result of the intervention

- Documentation of the hospital lethality and the non-fatal serious complications (Spinal Cord Ischemia, SCI, Stroke, TIA, high blood loss etc.)

- Documentation of medication at hospital discharge

- Documentation of long-term lethality and non-fatal serious complications (SCI, Stroke, TIA, major bleeding etc.) as well as hospitalization, re-intervention rates and medicinal drug therapy after 30 days, 1, 3 & 5 years. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Aortic Dissection

Clinical Trial Details

NCT number	NCT01197651
Study type	Observational
Source	Stiftung Institut fuer Herzinfarktforschung
Contact
Status	Completed
Phase	N/A
Start date	October 2008
Completion date	October 2011

View Details

See also
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