Effectiveness of the Rapid Intravascular Start (RIVS) System Versus Conventional Catheter
NCT00914069 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 175
Last updated 2017-04-13
Summary
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.
Conditions
- Vascular Access Complication
Interventions
- DEVICE
-
RIVS vascular access
Access to peripheral vasculature
- DEVICE
-
Conventional vascular access
Vascular access using conventional venous access device
Sponsors & Collaborators
-
C. R. Bard
lead INDUSTRY
Principal Investigators
-
Jeffrey S Stuart, MD · Washington Outpatient Surgery Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 5 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-06-30
- Primary Completion
- 2013-07-31
- Completion
- 2013-08-31
Countries
- United States
Study Locations
More Related Trials
-
RECANA OUS - Recana Thrombectomy Catheter System for Venous Obstruction and Occlusion Study (RECANA-OUS-IRL)
NCT07095660 ·Status: RECRUITING ·Phase: NA
-
Observational Peripheral IV Insertion Study
NCT04762121 ·Status: WITHDRAWN
-
RIPT Feasibility Trial
NCT03070834 ·Status: COMPLETED ·Phase: NA
-
Vascular Access in Cancer Patients - PICC vs PORT in a Randomized Controlled Trial.
NCT01971021 ·Status: COMPLETED ·Phase: NA
-
Use of Vein Viewer for Insertion of Peripheral Venous Cannula in Pediatric Patients With Difficult Intravenous Access
NCT00935909 ·Status: COMPLETED
-
Micropuncture vs. Standard Common Femoral Artery Access
NCT02026180 ·Status: TERMINATED ·Phase: NA
-
RECANA OUS - Recana Thrombectomy Catheter System for Venous Obstruction and Occlusion Study (RECANA-OUS-UK)
NCT07219758 ·Status: RECRUITING ·Phase: NA
-
Using a Novel Algorithm to Improve the Retrieval Rate of Inferior Vena Cava Filters (iRetrieve Study)
NCT02160964 ·Status: UNKNOWN
-
Impact of Availability of Showerpatch for Patients With Intravenous Catheters
NCT02324868 ·Status: TERMINATED ·Phase: NA
-
Safe-Infusion Study
NCT06727240 ·Status: RECRUITING ·Phase: NA
-
Innovative Central Line Securement Device in the Pediatric Population
NCT04522778 ·Status: TERMINATED ·Phase: NA
-
Iterative PICC Placement Versus Long Term Device
NCT02784730 ·Status: WITHDRAWN ·Phase: PHASE3
-
Comparative Study Between Foley and T-Control® Catheter in Patients With Long-term Catheterization
NCT05860231 ·Status: SUSPENDED ·Phase: NA
-
Trial Comparing Peripheral I.V. Catheter Complication Rates of Two Different Catheter Dressings
NCT02725788 ·Status: TERMINATED ·Phase: NA
-
An Innovative Taping Technique for Improved Intravenous (IV) Catheter Securement
NCT05948878 ·Status: COMPLETED ·Phase: NA
-
Filter Initial & Long Term Evaluation After Placement and Retrieval Registry
NCT01158482 ·Status: RECRUITING
-
Improved Outcomes With Pre-Procedure Shockwave IVL of Common Femoral Artery Access Site Prior to Large Bore Access and Pre-Closure
NCT07205068 ·Status: RECRUITING ·Phase: NA
-
The Clinical Efficacy of Midline Catheters
NCT03457259 ·Status: COMPLETED ·Phase: NA
-
Veinplicity for Improved Venous Access: The VIVA Trial
NCT03752632 ·Status: TERMINATED ·Phase: PHASE3
-
Ease of Use and Blood Clotting for the Gambro Polyflux HD-C4 Big Dialyzer
NCT00659724 ·Status: COMPLETED
-
A Feasibility Study Evaluating the Use of SafeBreak Vascular in the Geriatric Trauma Population
NCT03505957 ·Status: COMPLETED ·Phase: NA
-
Maintaining Patency in BioFlo Implanted Port Catheters With Saline Only Flushes
NCT02923830 ·Status: TERMINATED ·Phase: PHASE4
-
Peripheral Intravenous Catheter Complication Rate Comparison of Two Different Catheter-Stabilization Systems
NCT01382524 ·Status: COMPLETED
-
Catheter Resistance Monitoring to Predict Catheter-Associated Adverse Events in Children and Adolescents
NCT01737554 ·Status: COMPLETED
-
Compact Closed System Versus Mounted Open System (COSMOS)
NCT00665886 ·Status: COMPLETED ·Phase: PHASE4