Endovascular Abdominal Aortic Aneurysm Repair by Interventional Cardiologists

Endovascular Abdominal Aortic Aneurysm Repair (EVAR) Clinical Trial

— EVAR  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01452620
• Other study ID #: 11-10-01
• Status: Completed
• Phase: N/A
• First received: October 12, 2011
• Last updated: October 14, 2011
• Start date: January 2011
• Est. completion date: May 2011

Study information

• Verified date: October 2011
• Source: St. Joseph Mercy Oakland Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Registry for Endovascular repair of abdominal aortic aneurysm performed primarily by Interventional Cardiologists

Recruitment information / eligibility

• Status: Completed
• Enrollment: 170
• Est. completion date: May 2011
• Est. primary completion date: May 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with abdominal aortic aneurysm amenable for endovascular repair

Exclusion Criteria:

• Pregnant patients

• Patients less than 18 years old.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Aneurysm
• Aortic Aneurysm
• Aortic Aneurysm, Abdominal
• Endovascular Abdominal Aortic Aneurysm Repair (EVAR)

Locations

Country	Name	City	State
United States	St. Joseph Mercy Oakland Hospital	Pontiac	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
St. Joseph Mercy Oakland Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality		mean follow up, 30 months	Yes
Secondary	Complications	Peri-procedural (30 day) and follow up complications	mean follow up, 30 months	Yes