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Aortic-Stent-Register

I

Institute for Heart Attack Research Foundation (IHF)

Status

Completed

Conditions

Aortic Dissection

Study type

Observational

Funder types

Other

Identifiers

NCT01197651
Aortenstent

Details and patient eligibility

About

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:

Full 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.

Enrollment

199 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with significant illness of the distal thoracal aorta (distal Aortic-dissection; TAA; penetrated ulcer; covered perforation; traumatically transection of the distal thoracal aorta) including those that receive an endovascular stent or an open surgical operation.

Exclusion criteria

  • Missing signed informed consent

Trial contacts and locations

8

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Data sourced from clinicaltrials.gov

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