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OpenTrials
Completed

NCT Number: NCT02438605

Dynamic CT Imaging After Nellix Endoprosthesis Implantation

The Nellix Endovascular Sealing Prosthesis (EVAS) endoprosthesis is a new device aimed at prophylactic treatment of abdominal aortic aneurysms. In regular follow up conventional CT-imaging is used for surveillance. In this study dynamic CT imaging in patients pre- and post-operative will be assessed for device changes and anatomical variances.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Rijnstate Hospital

Arnhem, 6815AD, Netherlands

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Nellix implantation

Exclusion criteria

  • Use of chimneys or combined with other stent graft material

Treatment and study plan

Nellix

Device

Primary outcomes

  1. Changes in aortic aneurysm morphology as seen on dynamic CT after EVAS

    Time frame: 1 month

Secondary outcomes

  1. Dynamic changes in neck morphology after EVAS

    Time frame: 1 month

  2. Dynamic changes in common iliac artery morphology after EVAS.

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

Rijnstate Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
May 8, 2015
Registry last updated
Jul 1, 2016

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.

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