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NCT ID: NCT01570283 Completed - Viral Infection Clinical Trials

ARMS - Rapidly Generated Multivirus-Specific CTLs for Prophylaxis & Treatment of EBV, CMV, Adenovirus, HHV6 & BK Virus

ARMS
Start date: September 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The subjects eligible for this trial have a type of blood cell cancer, other blood disease or a genetic disease for which they will receive a stem cell transplant. The donor of the stem cells will be either the subject's brother or sister, or another relative, or a closely matched unrelated donor. The Investigators are asking subjects to participate in this study which tests if blood cells from the subject's donor that have been grown in a special way, can prevent or be a effective treatment for early infection by five viruses - Epstein Barr virus (EBV), cytomegalovirus (CMV), adenovirus, BK virus (BKV) and human herpes virus 6 (HHV6). The Investigators have grown T cells from the subject's stem cell donor in the laboratory in a way that will train them to recognize the viruses and control them when the T cells are given after a transplant. This treatment with specially trained T cells (also called cytotoxic T cells or "CTLs") has had activity against three of these viruses (CMV, EBV and Adenovirus) in previous studies. In this study the Investigators want to see if they increase the number of viruses that can be targeted to include BKV and HHV6 using a simple and fast approach to make the cells. The Investigators want to see if they can use a kind of white blood cell called T lymphocytes (or T cells) to prevent and treat adenovirus, CMV, EBV, BKV and HHV6 in the early stages of reactivation or infection.

NCT ID: NCT01566734 Completed - Clinical trials for Surgical Site Infections

Effect of Cefazolin and Normal Saline Irrigation on Surgical Site Infections (SSIs)

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

This study conducted to assess the effects of normal saline or cefazolin irrigation on the incidence of SSIs. Hypothesis: Normal saline or cefazolin irrigation decreases the incidence of SSIs.

NCT ID: NCT01566643 Recruiting - Clinical trials for Helicobacter Pylori Infection

Rabeprazole Based Sequential-Concommitant Hybrid Therapies for H. Pylori Infections

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

This prospective controlled randomized open-label clinical trial is designed to determine the optimal eradication rate of rabeprazole based sequential-concommitant hybrid therapies for adults infected with Helicobacter pylori in Eastern Taiwan. Enrolled patients will receive 3, 5 or 7 days of pre-concommitant (sequential part) treatment with rabeprazole + amoxicillin, then 7 days of concommitant treatment with rabeprazole + amoxicillin + clarithromycin + metronidazole.

NCT ID: NCT01565798 Completed - Clinical trials for Healthcare-acquired Infection

Efficacy Of Copper To Reduce Acquisition Of Microbes and Healthcare-acquired Infections

Start date: July 2010
Phase: N/A
Study type: Interventional

CONTEXT: Healthcare-acquired infections (HAI) cause substantial patient morbidity and mortality. Commonly touched items in the patient care environment harbor microorganisms that may contribute to HAI risk. Thus, reduction in the surface bioburden may be an effective strategy to reduce HAI. Inherent biocidal capabilities of copper surfaces offer a theoretical advantage to conventional cleaning, as disinfection is continuous rather than episodic. OBJECTIVE: Determine whether placement of copper-alloy surfaced objects in an intensive care unit (ICU) reduce risk of HAI. DESIGN: An intention to treat study where patients are sequentially placed into rooms with or without copper-alloy surfaced objects. SETTING: The ICUs of three hospitals, a tertiary academic hospital, an academic cancer center, and a Veteran's Administration Medical Center. PATIENTS: Any patient 18 years of age or older who required admission to an ICU at a study hospital is eligible for placement into a study room if available. INTERVENTION: Placement of copper-alloy surfaced objects in an ICU room. MAIN OUTCOME MEASURE: Rate of incident HAI and/or colonization with methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant Enterococcus (VRE) in each type of room.

NCT ID: NCT01564758 Completed - Clinical trials for Gram-Positive Bacterial Infections

Post Marketing Surveillance Study on Linezolid

A5951090
Start date: February 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine if Linezolid is safe for adult Filipino patients diagnosed with gram positive infections.

NCT ID: NCT01564615 Completed - Clinical trials for Catheter-Related Infections

AgION Catheter for Preventing Catheter-Related Bloodstream Infections

Start date: July 2007
Phase: N/A
Study type: Interventional

The investigators assessed if use of AgION-impregnated umbilical catheters can decrease the occurrence of catheter-related bloodstream infections (CRBSI) in preterm infants.

NCT ID: NCT01563406 Completed - Clinical trials for Catheter-related Bloodstream Infection

Hub Cleansing to Prevent Hub Infection

HUC-PHIN
Start date: March 2012
Phase: N/A
Study type: Interventional

Central venous catheter infections are common preventable adverse events among hospital patients. Microbes may enter catheter hubs, also known as needleless connectors, and result in downstream contamination. This study aims to compare alcohol disinfection of catheter hubs to disinfection with chlorhexidine gluconate in alcohol, which has been proven to be a superior disinfectant at the site of central venous catheter insertion. Scrub duration of central venous catheter hubs will also be evaluated.

NCT ID: NCT01562769 Terminated - Clinical trials for Patients Hospitalized in Infectious Disease

Interest of Contact Precautions for Preventing Micro-organisms Acquisition in Patients Hospitalized in Infectious Disease Unit of University-affiliated Hospital in Rennes

ISOL/STAND
Start date: March 2012
Phase: N/A
Study type: Observational

Application of isolation (=contact precautions) in hospitalized patients is recommended when patient is colonized (or infected) by micro-organism known for its outbreak capacity or high pathogenicity. It allows the reinforcement of universal precautions (=standard precautions) in order to control patient-to-patient micro-organisms transmission. Recently, the efficacy of this measure is questioned and its impact on patient care seems deleterious. In a particular context of Infectious Disease Unit, where standard precautions are handled (favorable architecture and appropriate practice for hand hygiene), assessment of contact precautions to reduce the incidence of acquired bacteria during hospitalization would be of interest. The investigators design a non-inferiority comparative study to measure the colonization pressure in patients hospitalized in two different parts of the department: one unit only with standard precautions applied (intervention) and one unit with contact precautions (control) as current routine care.

NCT ID: NCT01561248 Completed - Clinical trials for Hemolytic Uremic Syndrome

Study of Repetitive Intestinal Lavage in Patients With EHEC Associated Hemorrhagic Colitis

EHEC-PEG
Start date: May 2011
Phase: N/A
Study type: Interventional

The investigators examined the outcome of patients with severe Enterohaemorrhagic E. Coli (EHEC) O104:H4 infection suffering from bloody diarrhoea that were at risk to develop hemolytic uremic syndrome and underwent repetitive whole bowl lavage during hospitalization.

NCT ID: NCT01560468 Terminated - Clinical trials for Hepatitis C Infection

Study of Hepatitis C Virus (HCV) Entry Inhibitor in Liver Transplant Recipients With HCV Infection

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This study will test the safety and tolerability of HCV Entry Inhibitor ITX 5061 in Liver Transplant Recipients with Hepatitis C infection. The investigators hypothesize that ITX 5061 oral monotherapy will be safe in adults during and after liver transplantation and that therapy will also inhibit HCV infection of newly transplanted livers in adults with prior HCV infection.