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Clinical Trials/NCT03312127
NCT03312127
Terminated
Not Applicable

Evaluation of Peri-surgical Results at Short and Mean Terms of the GORE ® Excluder Iliac Branch Endoprosthesis

University Hospital, Toulouse1 site in 1 country3 target enrollmentAugust 1, 2017
ConditionsIliac Aneurysm

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Iliac Aneurysm
Sponsor
University Hospital, Toulouse
Enrollment
3
Locations
1
Primary Endpoint
Primary permeability maintenance of the iliac branch endoprosthesis, following its insertion (binary criterion)
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

The aim of this project is to demonstrate the benefit of the use of aortic iliac branch endoprosthesis in the iliac aneurysms and to avoid the classic complications.

Registry
clinicaltrials.gov
Start Date
August 1, 2017
End Date
July 26, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • High surgical risk:
  • Comorbidity cardiopulmonary
  • Renal insufficiency
  • Hostile abdomen including ascites or portal hypertension
  • Anatomic criteria:
  • Primitive iliac aneurysm superior to 25 mm without collar
  • Primitive iliac length superior to 40 mm
  • Primitive iliac distal diameter superior to 14 mm
  • Presence of internal iliac collar
  • Affiliation to a social security system

Exclusion Criteria

  • Patient without surgical risk
  • Non-respect of the Anatomic criteria
  • Patient with known allergy to the materials of the device
  • Patient with systemic infection
  • Patient with severe renal insufficiency
  • Patient unable to complete the oximetry test
  • Persons under legal protection

Outcomes

Primary Outcomes

Primary permeability maintenance of the iliac branch endoprosthesis, following its insertion (binary criterion)

Time Frame: at 12 months after surgery

Primary permeability maintenance of the iliac branch endoprosthesis, following its insertion. It is a binary criterion (permeable or not) This criterion will be evaluated by a doppler ultrasound. These exams will be performed by a unique vascular physician, who will measure the hemodynamic criterions and the associated gluteal region oximetry. Endoprosthesis will be considered to be permeable if the patient is asymptomatic (absence of gluteal claudication), if Doppler ultrasound and angio-scan confirm the permeability of the endoprosthesis. Primary permeability will be considered non-maintained at 1 year if a stenosis \>70% or a thrombosis of the hypogastric branch is observed by ultra-sound scan at a follow-up visit during the first year after surgery or at a ultra-sound scan exam motivated by pelvic ischemia clinical signs

Secondary Outcomes

  • Morbidity(peri-operative, at short term (3 months), mean-term (12 months))

Study Sites (1)

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