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Catheter-Related Infections clinical trials

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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: NCT02484287 Terminated - Clinical trials for Catheter Related Infections

Quality Control: A Prospective Analysis of EVD Effectiveness

Start date: April 2016
Phase: N/A
Study type: Interventional

The purpose and/or hypothesis: To decrease the amount of external ventricular drain (EVD) related catheter infections by comparing the efficacy of Oklahoma University Medicine standard EVD catheters, both impregnated and non-impregnated, in three principle areas: incidence of infection, cost analysis, and average durations of placement, all while maintaining the standards of technique.

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: NCT02358993 Completed - Clinical trials for Urinary Tract Infections

Short-course Methenamine Hippurate for Prevention of Post-operative UTI

NO-UTI
Start date: December 2014
Phase: N/A
Study type: Interventional

The investigators will determine the efficacy of an innovative short regimen of methenamine hippurate on prevention of post-operative UTI in patients requiring short-term catheterization after pelvic reconstructive surgery through a single-blind, randomized controlled trial. Primary outcome will be the rate of symptomatic UTI within 3 weeks of catheter removal. The investigators will study cost-effectiveness, antibiotic resistance profiles, and adverse drug effects. Findings may reduce antibiotic use and nosocomial UTIs.

NCT ID: NCT02279121 Completed - Clinical trials for Catheter-Related Infections

ATAPAC Study (TauroLock Activity in Adult Cancer Patients)

ATAPAC
Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of a lock taurolidine-citrate solution vs standard saline solution for primary prevention of central venous catheter-associated bloodstream infection in adult patients treated with intra-venous therapy for a solid tumor

NCT ID: NCT02077816 Completed - Infection Clinical Trials

Using a Infrared Thermometer to the Early Detection of Catheter Related Infections

Start date: August 2011
Phase: N/A
Study type: Observational

This is a pilot study which aims to show the temperatures measured on body surface with an infrared thermometer on inpatients who need a central venous catheter (CVC) for medical care. Because the local temperature could be altered, at least during local infectious processes, seems to be reasonable to think that this approach could be helpful to its early diagnosis.

NCT ID: NCT01947751 Recruiting - Clinical trials for Catheter Related Infection

Catheter Early Withdrawal or Maintenance in Sepsis or Septic Shock

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

Central venous catheter(CVC)-related infection is an inherent complication of this device that should be treated promptly. However, there are doubts about the need for the immediate withdrawal of CVC while there is still no confirmation of such infection. The aim of this study is to compare the resolution of CVC-related infection, testing two approaches: catheter´s early exchange, when the possibility of related sepsis is considered, versus the maintenance of the CVC and early antibiotic therapy until the infection is confirmed.

NCT ID: NCT01820962 Terminated - Thrombosis Clinical Trials

Concentrated Citrate Locking to Reduce the Incidence of CVC-related Complications in Hematological Patients

Start date: July 2006
Phase: Phase 3
Study type: Interventional

Patients with a hematological malignancy who are undergoing intensive chemotherapy need a central venous catheter (CVC)during their treatment. CVCs are locked with heparin when they are not used. The purpose of this study is to determine whether concentrated citrate locking, compared to heparin, reduces the incidence of central venous catheter-related thrombosis and infections in patients with hematological malignancies undergoing intensive chemotherapy.

NCT ID: NCT01772875 Withdrawn - Clinical trials for Catheter Related Infections

Bladder Lavage as Decontamination Method for Asymptomatic Bacteriuria With Uropathogens in Catheterized Patients

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

In patients with advanced multiple sclerosis, permanent urinary catheters are often used to manage the urinary incontinence and bladder emptying problems. These catheters will lead to urinary tract infection, blocking of the catheter etc.. Especially infections with certain bacteria such as proteus, enterobacteriaceae and ESBL producing enterobacteriaceae and pseudomonas can pose a problem for the hospital infection control and for the patient. This study wants to evaluate the potential role of regular bladder lavage with saline, a solution of betadine, an acid solution of acetic acid and of URotainer Twin Suby G ( Braun)in the decontamination of these bladders and the prevention of clinically relevant urinary tract infections.

NCT ID: NCT01696227 Completed - Clinical trials for Catheter-Related Infections

Novel Probiotic Treatment for Prevention of Recurrent UTIs in Children

Nissle 1917
Start date: July 2012
Phase: N/A
Study type: Observational

Background: Urinary tract infections (UTIs) are a common and costly cause of doctor visits for children. Frequent UTIs trigger kidney damage that leads to serious diseases like high blood pressure, pregnancy complications, and kidney failure. Treating UTIs with preventative antibiotics has not shown improvement of the risk of these diseases, and contributes to the growing public health issue of antibiotic resistant bacteria. Bacteria that cause UTIs originate from the bowel. In an effort to reduce the number of UTIs, investigators want to exchange the bacteria living in our bowels for a more harmless variety. Hypothesis and specific aims: Investigators hypothesize a probiotic comprised of a probiotic bacteria will change the bowel bacteria, thereby reducing the numbers of infection-causing bacteria, thus reducing frequency of UTIs in healthy patients with recurrent UTIs and those patients with urinary tract problems that require use of catheters to empty their bladders. Aim 1: Investigators plan to challenge infection-causing bacteria like Pseudomonas species, Enterococcus species, and Klebsiella species to live in the same environment with the probiotic bacteria to see how the numbers of each bacteria change. Aim 2: Investigators will culture bacteria that live on urinary catheters and then challenge them to live in the same environment as the probiotic bacteria. Potential Impact: This novel treatment prevents UTIs by exchanging a patient's bowel bacteria for a harmless bacteria and reduces the use of antibiotics overall in the community.