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Central Venous Catheter clinical trials

View clinical trials related to Central Venous Catheter.

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NCT ID: NCT04302376 Completed - Clinical trials for Central Venous Catheter Thrombosis

Thrombotic Complications After Central Venous Catheterization

TARZAN
Start date: December 1, 2019
Phase:
Study type: Observational

Rationale: Complications related to central venous catheterization are mechanical, infectious or thrombotic in origin. Potential complications of catheter-related thrombosis are not insubstantial and include pulmonary embolism, post-thrombotic syndrome or thrombophlebitis. Prevalence and incidence of catheter-related thrombosis at the intensive care unit is unclear and treatment, especially of asymptomatic thrombosis, remains ambiguous. Therefore a study is warranted that evaluates the prevalence and incidence of catheter-related thrombosis and investigates its potential consequences. We hypothesize that the incidence of catheter-related thrombosis is 5-15%. Objective: To assess the prevalence and incidence of symptomatic and asymptomatic catheter-related thrombosis.

NCT ID: NCT04256564 Not yet recruiting - Clinical trials for Central Venous Catheter Placement

Comparison of Two Syringe-free In-plane Techniques in Ultrasound-guided Central Venous Catheterization

Start date: March 2020
Phase: N/A
Study type: Interventional

Ultrasound guidance has become a standard for central venous catheterization. The aim of this study is to compare jugular venous catheterization by using lateral oblique approach to brachiocephalic catheterization by using Y-shape imaging. The trial is planned as prospective randomized and single-blind study. Eighty patients are planned to include in this study. Patients will be assigned to two groups: Oblique visualization Group (central catheter will be placed to the jugular vein by using ultrasound-guided in-plane syringe-free technique) and Y-shape visualization Group (central catheter will be placed to the brachiocephalic vein by using ultrasound-guided in-plane syringe-free technique). Two groups will be compared in terms of number of puncture attempts, procedural time, time of preprocedural ultrasound scanning, overall success rate, complications, the ease of the catheterization process and ultrasound visibility.

NCT ID: NCT04117776 Completed - Clinical trials for Central Venous Catheter

Skin Decolonization of Children Hospitalized in Intensive Care Unit

DCpedrea
Start date: January 17, 2020
Phase:
Study type: Observational

The purpose of this study is to evaluate the efficacy and duration of the skin decolonization brought by a daily wash using Chlorhexidine Gluconate 2% pad compared to a standard wash with mild soap in children hospitalized in intensive care unit.

NCT ID: NCT03879954 Completed - Clinical trials for Central Venous Catheter

US-guided OOP Internal Jugular Vein Vs IP Supraclavicular Subclavian Vein Catheterization in ICU

IPSSCVC
Start date: February 26, 2019
Phase: N/A
Study type: Interventional

Patients were randomly divided into two groups: ultrasound-guided (US-guided) out-of-plane internal jugular vein (OOP-IJV) and in-plane supraclavicular subclavian vein (IP-SSV) catheterization. For OOP-IJV cannulation, the transducer was placed to identify IJV in short-axis view. The needle was introduced at an angle of 60° to the skin surface, and advanced under real-time US guidance until visualizing the tip of the needle inside the vein. For IP-SSV cannulation, a short-axis view of the IJV was obtained first. The probe was slid caudally following the IJV until getting the best long-axis view of the SCV. Using an in-plane approach, the needle was inserted at the base of the transducer at a 30° angle and advanced under the long axis under real-time US guidance targeting the SCV.

NCT ID: NCT03841240 Enrolling by invitation - Clinical trials for Catheter-Related Infections

The Central Venous Catheter Related Complications in Critically Ill Patients

Start date: February 19, 2019
Phase:
Study type: Observational

In this prospective clinical study, the researchers investigate the incidence of catheter-related thrombosis and catheter-related infection during indwelling central venous catheterization in critically ill patients, and analyzed the risk factors for catheter-related complications and the relationship between catheter-related thrombi and catheter-related infections. The sample size is about 500.

NCT ID: NCT03812757 Completed - Clinical trials for Central Venous Catheter Placement

Supraclavicular Fossa US View for Catheter Positioning in Right Subclavian Central Venous Catheterization

Start date: January 18, 2019
Phase:
Study type: Observational [Patient Registry]

The study will evaluate if the supraclavicular fossa ultrasound view can be used to achieve a correct catheter tip placement in infraclavicular right subclavian central venous catheter placement. This may make routine post-procedural x-ray exams redundant.

NCT ID: NCT03801811 Recruiting - Clinical trials for Central Venous Catheter

Use of the Skin Glue in the Placement of Central Venous Catheters Port a Catch

Port glue cvc
Start date: September 5, 2018
Phase:
Study type: Observational

The use of glue as a device in the implantation of central venous catheters has recently been introduced into European clinical practice, initially with the aim of blocking bleeding at the point of exit of the PICCs, but at the same time also to close the cutaneous incision practiced to create the PORT positioning pocket. It is possible that the surgical incision created for the insertion of the PORT may undergo complications such as: local bleeding, infections or wounds of the surgical wound. A solution to this problem could be the application of the cyanoacrylate dermal glue on the edges of the surgical wound, after intradermal suture. The glue would have the purpose of sealing the surgical wound so as to immediately seal the skin incision with hemostatic effect and create a potential barrier against infections.

NCT ID: NCT03766828 Completed - Clinical trials for Central Venous Catheter Thrombosis

Dialysis Catheter Placement in Patients With Thoracic Central Venous Occlusion

Start date: September 1, 2016
Phase:
Study type: Observational

A unique inside-out-access technique with a new CE certified device (Surfacer (R) Bluegrass Vascular, San Antonio, Tx, USA) enables repetitive and confident right-sided placement of central venous catheters in hemodialysis patients with thoracic central venous occlusion.

NCT ID: NCT03683563 Recruiting - Renal Dialysis Clinical Trials

The Impact of Different Citrate Concentrations as Locking Solutions on Development of Biofilm and Function of Hemodialysis Catheters

Start date: April 11, 2018
Phase: N/A
Study type: Interventional

Evidence that supports using certain concentration of trisodium citrate as a locking solution for hemodialysis catheters has not yet been established. Higher concentrations of trisodium citrate are more effective in preventing thrombosis, formation of blood clots, preventing infections and biofilm formation, but due to potential side effects, their use is limited. The aim of the study is to compare the impact of two different concentrations of tri-sodium citrate solution (30% and 4%) on the formation of biofilms in hemodialysis single-volume jugular hemodialysis catheters and to determine the effectiveness of prevention of dysfunction of hemodialysis catheters.

NCT ID: NCT03672006 Completed - Clinical trials for Central Venous Catheter Thrombosis

t-PA Prophylaxis to Prevent Catheter-associated Thrombosis and Infection

TOPCAT
Start date: April 22, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this pilot study is to test feasibility of concept, consent and enrollment rates, and mechanics of study designed to assess if intra-catheter dwells of tissue plasminogen activator (t-PA) is effective in decreasing the rate of clinically diagnosed central line associated blood stream infection (CLABSI) or venous thromboembolism (VTE) in central venous catheters (CVC) compared to standard of care heparin dwell.