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Vascular Access Complication clinical trials

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NCT ID: NCT01937195 Recruiting - Clinical trials for Vascular Access Complication

AccuCath™ Intravenous Catheter System Compared to Conventional Peripheral Intravenous Catheters

Start date: April 2013
Phase: N/A
Study type: Interventional

The study will test a hypothesis that the AccuCath™ System will have a higher rate of successful first attempt PIV placement, higher completion of therapy, fewer complications, longer dwell times and higher user satisfaction compared to Conventional IV Catheters.

NCT ID: NCT01927185 Completed - Clinical trials for Perioperative/Postoperative Complications

Long-versus Short-Axis Ultrasound Guidance for Subclavian Vein Cannulation

Start date: June 2013
Phase: N/A
Study type: Interventional

Central venous catheterization is commonly applied in patients undergoing cardiac surgery. The subclavian vein has lower risk of infection and provides more patients comfort. However central venous catheterization may results in complications such as pneumothorax, hemothorax or arterial puncture. It has been suggested that ultrasound (US) guidance could improve the success rate, reduce the number of needle passes and decrease complications. Two different real-time 2-dimensional US techniques can be employed in the insertion of central venous catheters. The first technique involves real-time US-guided cannulation of subclavian vein using a long axis/in-plane approach. The second one involves real-time US-guided using a short axis/out-off-plane approach. However to date no studies have compared their efficacy and safety. The purpose of this study was to compare the US-guided long-axis versus short-axis approach for the SCV catheterization in adult critical care patients.

NCT ID: NCT01911403 Terminated - Clinical trials for Vascular Access Complication

AGIR Study: Angio-Seal in Interventional Radiology

AGIR
Start date: December 2010
Phase: N/A
Study type: Interventional

Clinical study in patients undergoing any intervention requiring vascular access to the femoral artery. The study compares Angio-Seal™ vs. Manual Compression with regard to control the vascular access. It is designed to demonstrate superiority of the Angio-Seal™ with an unchanged risk-profile.

NCT ID: NCT01794325 Completed - Clinical trials for Coronary Heart Disease

Transradial and Transfemoral Coronary Angiography by EXPERienced operaTors

EXPERT
Start date: February 2013
Phase: N/A
Study type: Interventional

Transradial approach (TRA) reduces vascular complications and access related-bleeding compared to transfemoral approach (TFA). However, this technique has been related to higher radiation exposure during coronary angiography and percutaneous coronary intervention. Previous studies have shown that TRA demands a long learning curve, and procedure success rate increases with operator's experience. Our hypothesis is that the higher radiation exposure during TRA is not a technique issue, but due to operator's expertise. The aim of this study is to evaluate whether experienced operators with either TRA or TFA can perform diagnostic coronary angiography with similar radiation exposure.

NCT ID: NCT01763801 Completed - Clinical trials for Vascular Access Complication

Optimization of EKG Method for Long Term Central Venous Catheter Tip Placement

Start date: July 2011
Phase: Phase 4
Study type: Interventional

Intravenous electrocardiographic guidance (IVECG) is a safe, reliable and accurate technique to correctly position the catheter tip. The investigators sought to evaluate the superiority of the P-maximal (P-max) wave compared to the P-submaximal (P-submax) wave in obtaining a more correct, safer and longer lasting device placement, with a lower incidence of complications and secondary misplacement.

NCT ID: NCT01446263 Completed - Clinical trials for Vascular Access Complication

RADIAL Versus Femoral Access for Coronary Artery Bypass Graft Angiography and Intervention (RADIAL-CABG) Trial

RADIAL-CABG
Start date: October 2011
Phase: Phase 3
Study type: Interventional

Increased use of radial access for cardiac catheterization is being advocated because studies have showed lower arterial access related complication rates and higher patient satisfaction as compared to femoral access. However, little is known on patients with prior coronary artery bypass graft (CABG). The RADIAL CABG Trial is a randomized-controlled trial proposed to test the hypothesis that bypass graft angiography and intervention via radial access provides lower vascular complication rates, similar contrast and equipment utilization and higher patient satisfaction when compared with transfemoral approach.

NCT ID: NCT00914069 Terminated - Clinical trials for Vascular Access Complication

Effectiveness of the Rapid Intravascular Start (RIVS) System Versus Conventional Catheter

Start date: June 2009
Phase: N/A
Study type: Interventional

The study will test a hypothesis that the RIVS system will have a higher rate of successful first PIV placement compared to conventional catheter without a significant increase in complications and time of procedure.