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Clinical Trials/JPRN-jRCTs052190096
JPRN-jRCTs052190096
Active, not recruiting
未知

Postoperative endovascular intervention for false lumen for aortic dissection - FL intervention

Matsuda Hitoshi0 sites15 target enrollmentJanuary 27, 2020
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ConditionsDissecting aneurysm of the aortaStanford classification, Aortic remodelingI710

Overview

Phase
未知
Intervention
Not specified
Conditions
Dissecting aneurysm of the aorta
Sponsor
Matsuda Hitoshi
Enrollment
15
Status
Active, not recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 27, 2020
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Matsuda Hitoshi

Eligibility Criteria

Inclusion Criteria

  • •Patients who had past history of undergoing the surgery for aortic dissection.
  • •Patients who developed aortic dilation more than 45mm in thoracic aortic aneurysm or more than 40mm in abdominal aortic aneurysm.
  • •Patients who developed rapid aortic dilation more than 3mm in 6 months or more than 5mm in 12months.

Exclusion Criteria

  • •Patients who had systemic infection that may increase the risk of device\-related infection.
  • •Patients who are allergic to the material of the device.
  • •Pregnant women, lactating women or women who cannot agree on contraception during participating in this study.

Outcomes

Primary Outcomes

Not specified

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