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Catheter-Related Infections clinical trials

View clinical trials related to Catheter-Related Infections.

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NCT ID: NCT03945045 Active, not recruiting - Venous Thrombosis Clinical Trials

A Study of the IJV or the SCV Approach for Ultrasound-guided Implantation of TIVAD

Start date: May 21, 2019
Phase: N/A
Study type: Interventional

To compare IJV and SCV as the implantation site of TIVAD and its associated thrombotic or occlusion rate, our study plans to enroll 240 patients with cancer who require central line TIVADs and randomizes them with 1:1 ratio to receive the TIVAD implantation at SCV or IJV. After the implantation, the patients will be regularly followed through phone contact and chart review for 2 years, and any symptomatic thrombosis or occlusion will be found during chemotherapy injection or regular push-pull heparin saline flush every 6 weeks as our hospital care protocol. To detect any asymptomatic thrombosis, the patients will also receive screening vascular ultrasound at 2 weeks, 2 months, and 6 months postoperatively. The study primary endpoints include any infection, asymptomatic thrombosis found by screen ultrasound, and clinically symptomatic thrombosis or occlusion and major mechanical failure/dislocation of TIVAD.

NCT ID: NCT02515201 Active, not recruiting - Clinical trials for Catheter-Related Infections

Heparin Versus Taurolidine to Bloodstream Infection Prevention Related in Central Venous Catheter in Children

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Clinical trial, that aim is evaluation of the use of taurolidine and heparin in the prevention of bloodstream infection in venous catheter in children with intestinal failure.

NCT ID: NCT02472158 Active, not recruiting - Clinical trials for Catheter-Related Infections

Chlorhexidine-Impregnated Sponge Dressing: A Clinical Trial

CISDCT
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the use of chlorhexidine-gel-impregnated dressing and the transparent polyurethane film dressing as coverage of the site of insertion of central venous catheter, in the evaluation of catheter colonization in critically ill adults patients.

NCT ID: NCT01592032 Active, not recruiting - Clinical trials for Catheter-Related Infections

Concentration of Antimicrobials in Catheter-lock Solutions

CONAN
Start date: May 2012
Phase: Phase 4
Study type: Interventional

The antibiotic lock technique (ALT) is used as local treatment for Catheter-Related Bacteremia (CRB). It consists in the administration of a concentrated antimicrobial solution with a calculated volume to fill the lumen of the catheter. The lock solution is indwelled within the catheter for a defined period of hours or days before been removed. Currently, the Infectious Diseases Society of America (IDSA) Guidelines for treatment and management of CRB, recommends to change the antibiotic solution every 24 hours. The investigators expect to determine the stability of the concentration of vancomycin, teicoplanin, linezolid, daptomycin and tigecycline used in lock solutions, and thus to assay the optimal timeframe that the concentration of antibiotic used in lock solution keeps its in vivo antimicrobial activity. Study Hypothesis: An antibiotic lock solution maintains in vivo concentration and antimicrobial activity for at least 10 days after its infusion inside a subcutaneous port catheter.