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Endovascular Device
FDA Approved EVAR AAA Graft Systems for Abdominal Aortic Aneurysm (LEOPARD Trial)
N/A
Waitlist Available
Led By Christopher Kwolek, MD
Research Sponsored by Endologix
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to five years
Awards & highlights
LEOPARD Trial Summary
This trial is comparing the Endologix AFX endovascular AAA system with anatomical fixation against other approved Endovascular systems with proximal fixation, to see which is better.
Eligible Conditions
- Abdominal Aortic Aneurysm
LEOPARD Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to five years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to five years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
AIDS related complex
Secondary outcome measures
Loss of Neck Apposition as Measured by Length in mm
Number of AAA Related Secondary Procedures
Number of Adjunctive Procedures Necessitated During the Implant Procedure.
+5 moreLEOPARD Trial Design
2Treatment groups
Active Control
Group I: FDA Approved EVAR AAA Graft SystemsActive Control1 Intervention
Subjects randomized to receive the comparator AAA Endovascular Graft System for implantation to repair Abdominal Aortic Aneurysm via femoral access.
Group II: AFX EVAR AAA Graft SystemActive Control1 Intervention
Subjects randomized to receive the Endologix AFX Endovascular Graft System for implantation to repair Abdominal Aortic Aneurysm via femoral access.
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Who is running the clinical trial?
EndologixLead Sponsor
22 Previous Clinical Trials
3,517 Total Patients Enrolled
Christopher Kwolek, MDPrincipal InvestigatorEndologix
4 Previous Clinical Trials
1,498 Total Patients Enrolled
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