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Aorta Dynamics after Endovascular Aorta Repair

Aorta Dynamics after Endovascular Aorta Repair

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24172
Enrollment
40
Registered
2020-02-21
Start date
2020-04-01
Completion date
Unknown
Last updated
2024-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

thoracic aorta pathology

Interventions

Present practise is that the patients undergo CTA of the aorta pre-operatively and post-operatively before discharge or after 6 to 8 weeks, after 3 to 6 months, after 12 months, and yearly thereafter.

Sponsors

University of Twente
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Asymptomatic thoracic aortic pathology • Age > 65 years • Indication for aortic pathology treatment according to standard practise • Anatomically suitability for one of the investigated grafts

Exclusion criteria

Exclusion criteria: • No informed consent obtained • eGFR < 30 ml/min • Allergy for intra venous contrast fluid

Design outcomes

Primary

MeasureTime frame
To gain insight in the parameters that influence the success and failure of the proximal fixation and/or sealing of Thoraflex Hybrid device and Relay(Branch) stent grafts. More practically, this leads to the questions of how the diameter of the (proximal) stent rings changes during the cardiac cycle (pulsatility), how the diameter changes over a period of several months (expansion) and how the grafts interact with the dynamics of the stented target vessels.

Secondary

MeasureTime frame
• How does the estimated vessel compliance change during follow-up? • Can we observe other kinds of motion that change over time? • What are the differences and similarities of thoracic endograft vs. thoracic hybrid graft (Relay(Branch) vs. Thoraflex Hybrid) considering: o Expansion? o Pulsatility? o Conformability to the native vessel?

Contacts

Public ContactJaimy Simmering

University of Twente

j.a.simmering@utwente.nl+31 53 489 8185

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)