NCT Number: NCT01710878
Performance and Safety of a Second Generation Antimicrobial Graft in Abdominal Position
Safety and performance of an anti-microbial vascular graft in the treatment of aneurysmal and occlusive disease of the abdominal aorta.
Looking for future studies?
Notify MeKey information
Conditions
Age range
18 year–85 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
CHRU, Angers, France
About this study
The purpose of this multi center, single arm study is to demonstrate the safety and performance of the Second Generation Anti-Microbial (InterGard Synergy) vascular graft in the treatment of aneurismal and occlusive diseases of the abdominal aorta.
The primary endpoint is the assessment of primary and secondary graft patency. The secondary endpoints were the assessment of adverse events and the assessment of triclosan and silver contents in the serum over the time.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patient aged 18-85 years
Patient presenting with an aorto-iliac occlusion (obstruction of flow) or stenosis, or aorto-iliac aneurysm and eligible for a revascularization with a bifurcated graft
Exclusion criteria
Patient treated as an emergency
Patient included in another investigation
Patient pregnant or lactating or woman of childbearing potential
Patient with a known allergy to the material device used (collagen, triclosan, silver)
Patient with previous aorto-iliac bypass or replacement
Treatment and study plan
Primary outcomes
-
Primary Graft Patency
Time frame: Up to 36 months
Defined as uniterrupted flow with no interventions. Follow-up timeframes - 1, 6, 12, 24, and 36 months
Secondary outcomes
-
Secondary endpoint - assessment of AEs
Time frame: Up to 36 months
Follow-up timeframes - 1, 6, 12, 24, and 36 months
Other outcomes
-
Secondary endpoint - levels of silver and triclosan
Time frame: Up to 30 days
Serum levels prior to surgery, 1 day post-implant, discharge and 30 days
Sponsors and collaborators
Lead sponsor
Maquet Cardiovascular
Industry
Registry information
Official study title
Multicenter Clinical Study Assessing the Performance and the Safety of the Second Generation Antimicrobial Graft in Abdominal Position
Acronym: SYNERGY
Important dates
- Study start
- 2008
- Primary completion
- 2010
- Study completion
- 2012
- First posted
- Oct 19, 2012
- Registry last updated
- Nov 26, 2013
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.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Circulating microRNAs and Degenerative Abdominal Aorta Aneurysm
NCT03974958
Abdominal Aorta Aneurysm, Aneurysm
Marseille, France
View Trial DetailsImpact of Intra- and Postoperative Continuous Infusion of Lidocaine on Analgesia in Vascular Anaesthesia
NCT04691726
Abdominal Aorta Aneurysm, Abdominal Aorta Atheroma
Katowice, Poland
View Trial DetailsFollow-up After Endovascular Repair of Abdominal Aortic Aneurysm
NCT00488943
Abdominal Aortic Aneurysm, Aneurysm
San Francisco, California, United States
View Trial DetailsNellix Registry Study: EVAS-Global
NCT02996396
Abdominal Aortic Aneurysm, Aneurysm
Augsburg, Germany
View Trial Details