Vascular No-React Graft Against Infection
NCT04031001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 43
Last updated 2023-12-21
Summary
This study seeks to demonstrate the effectiveness and safety of the Non-valved Conduit for CE marking on the basis of infection. The rationale for infection resistance with the conduit is that BioIntegral Surgical No-React® treated products have a well-documented history of infection resistance in hybrid vascular settings.
Conditions
- Vascular Infections
Interventions
- DEVICE
-
No-React Non-valved Conduit
Operative replacement of infected graft or implantation in infected area.
Sponsors & Collaborators
-
Catharina Ziekenhuis Eindhoven
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-12-22
- Primary Completion
- 2021-02-06
- Completion
- 2021-07-13
Countries
- Netherlands
Study Locations
More Related Trials
-
PowerAssert Radio-Frequency (RF) Guidewire Coronary In-Stent Chronic Total Occlusion (CTO)
NCT01131793 ·Status: COMPLETED ·Phase: PHASE2
-
European Aortic Data Collection Project
NCT05896397 ·Status: RECRUITING
-
MANTA Registry for Vascular Large-bore Closure
NCT03330002 ·Status: COMPLETED
-
Concave Supra-arch Branched Stent-Graft System for Endovascular Treatment of Aortic Arch Diseases
NCT06520774 ·Status: RECRUITING ·Phase: NA
-
The VIRTUE Post Marketing Surveillance Registry
NCT01213589 ·Status: COMPLETED
-
Safety Study to Evaluate Bilateral CNTF Implants in Subjects With MacTel Type 2
NCT04729972 ·Status: COMPLETED ·Phase: PHASE2
-
Self-Centering Guide Catheter Feasibility Study
NCT02639494 ·Status: COMPLETED ·Phase: NA
-
The Study to Evaluate Patient Outcome Using Distal Protection Combined With the BX Velocity.
NCT00264043 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Peripherally Inserted Central Catheter Placement by Interventional Radiologists Using the Sonic Flashlight
NCT00226213 ·Status: COMPLETED ·Phase: PHASE1
-
Prospective Multicenter Study to Characterize the REAL-WORLD EVIDENCE Regarding Safety and Performance of the PTCA Catheters Family
NCT05232565 ·Status: COMPLETED
-
Endurant™ Stent Graft System in the Treatment of Infra-renal Abdominal Aortic Aneurysms (ENDURANT France)
NCT01526811 ·Status: COMPLETED
-
CD0104 VEST II Post Marketing Surveillance Study
NCT02332330 ·Status: COMPLETED ·Phase: NA
-
Safety and Efficacy Study Of The Thoracic Aortic Stent Graft System Treating Aortic Dissection
NCT05430672 ·Status: UNKNOWN ·Phase: NA
-
Thoracoabdominal Artery Stent Graft System Exploratory Study
NCT06710938 ·Status: RECRUITING ·Phase: NA
-
Endurant Bifurcated and Aorto-Uni-Iliac (AUI) Stent Graft System
NCT00705718 ·Status: COMPLETED ·Phase: NA
-
EverFlex™ Self-expanding Peripheral Stent With Entrust™ Delivery System Clinical Study
NCT02066740 ·Status: COMPLETED ·Phase: NA
-
SoundBite™ Crossing System Pivotal Peripheral CTO Crossing Study
NCT03266835 ·Status: COMPLETED ·Phase: NA
-
Prospective Multicenter Study to Characterize the REAL-WORLD EVIDENCE Regarding Safety and Performance of the PTCA NC Catheters Family
NCT05536180 ·Status: COMPLETED
-
Safety and Efficacy Study of Iliac Bifurcation Stent Graft System
NCT03686189 ·Status: UNKNOWN ·Phase: NA
-
Safety and Efficacy Study of Abdominal Aortic Aneurysm Stent Graft System
NCT03687489 ·Status: UNKNOWN ·Phase: NA
-
ArterX Safety and Efficacy Study for Cardiac Indications
NCT01957904 ·Status: COMPLETED ·Phase: NA
-
CONTINuous Infra-Inguinal Stenting Using the Bard® LifeStent® VascUlar Stent SysteMs ("CONTINUUM")
NCT00908947 ·Status: TERMINATED ·Phase: NA
-
Bactiseal Catheter Safety Registry in China
NCT04496414 ·Status: COMPLETED
-
VEST Device to Enhance Safein Vein Patency
NCT06500897 ·Status: COMPLETED
-
Zenith Thoracic Alpha (ZTA) Post-Market Data Collection
NCT06094127 ·Status: ACTIVE_NOT_RECRUITING