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Infection clinical trials

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NCT ID: NCT03426488 Recruiting - Cancer Clinical Trials

Northern Sweden Health and Disease Study

NSHDS
Start date: January 1986
Phase: N/A
Study type: Observational

NSHDS (Northern Sweden Health and Disease Study) is an umbrella term for a prospective biobank with related survey data. The sample collection consists of three subcohorts, Västerbotten Intervention Programme (VIP), Mammography Screening Project (MA) and MONICA (MONItoring of Trends and Determinants in CArdiovascular Disease). The blood samples are stored at the Northern Sweden Biobank.

NCT ID: NCT03421743 Completed - Clinical trials for Mycobacterium Infections, Nontuberculous

Pilot Trial of Inhaled Molgramostim in Nontuberculous Mycobacterial (NTM) Infection

OPTIMA
Start date: March 1, 2018
Phase: Phase 2
Study type: Interventional

The trial is an open-label, non-controlled, multicenter, pilot clinical trial of inhaled molgramostim (recombinant human Granulocyte-Macrophage Colony Stimulating Factor; rhGM-CSF) in subjects with persistent pulmonary Nontuberculous Mycobacterial (NTM) infection. Subject will be treated for 24-weeks with inhaled molgramostim and will be followed up for 12-weeks after end of treatment. The primary aim of the trial is to investigate the efficacy of inhaled molgramostim on NTM sputum culture conversion to negative.

NCT ID: NCT03420599 Recruiting - Infection Clinical Trials

Microbiota is Related With Increasing Infection Rates After Splenectomy

Start date: May 1, 2017
Phase:
Study type: Observational

Studies has shown an increasingly infection rate after splenectomy, and there is a potential correlation between microbiota and immune system. investigators suppose that increasingly infection can be associated with the alteration composition of the gut microbiota after splenectomy. It's investigators' aim to discover if any difference of gut microbiota is exist in patients who suffer from traumatic splenectomy compared with normal people, ultimately aim toreduce and mitigation infection rate through controlling gut microbiota.

NCT ID: NCT03418571 Terminated - Clinical trials for Respiratory Syncytial Virus Lower Respiratory Tract Infection

Evaluation of ALX-0171 in Japanese Children Hospitalized for Respiratory Syncytial Virus Lower Respiratory Tract Infection

Start date: March 1, 2018
Phase: Phase 2
Study type: Interventional

This was a randomized, double-blind, multicenter, Phase II study (NCT03418571) designed to support the selection of an optimal dose of inhaled ALX-0171 for further clinical development, taking ethnicity into consideration. Based on the results of the Phase IIb dose-ranging study ALX0171-C201 (RESPIRE), the Sponsor decided to discontinue ALX-0171 development in infants and to early terminate the ALX0171-C203 study.

NCT ID: NCT03413293 Not yet recruiting - Clinical trials for Nosocomial Infection

Nosocomial Bacterial and Fungal Chest Infections in Cirrhotic Patients

Start date: June 2018
Phase:
Study type: Observational

Hospital acquired chest Infections are common complications in hospitalized cirrhotic patients. Infectious complications are the most common cause of mortality in cirrhotic patients with bronchopneumonia early antibiotic treatment at the base of culture and sensitivity is an optimal therapeutic approach in cirrhotics with nosocomial pneumonia Intensive care unit acquired pneumonia is the leading infection in critically ill patients and a major cause of morbidity and mortality despite recent major advances in antimicrobial therapy, supportive care, and the use of a broad range of preventive measures

NCT ID: NCT03411538 Completed - Clinical trials for Hospital-acquired Infections

Mortality Related to AMR in Patients With Hospital-acquired Infection

HAMR
Start date: March 1, 2018
Phase:
Study type: Observational

This is a prospective surveillance study to estimate excess deaths due to and risk factors associated with antibiotic-resistant infection among patients with hospital-acquired infection (HAI) in a resource-limited setting. We will focus on six pathogenic bacteria that are of clinically important in the hospital.

NCT ID: NCT03408782 Completed - Clinical trials for Surgical Site Infection

Drains and Surgical Site Infections

Start date: February 22, 2013
Phase: N/A
Study type: Observational

This prospective observational study examines the associations of presence, duration, type, number and location of surgical drains with the risk of surgical site infections in a contemporary and multicentric cohort of general, orthopedic trauma and vascular surgery procedures.

NCT ID: NCT03408626 Not yet recruiting - Clinical trials for Microbial Colonization

Microbiological Assessment After Chemo-Mechanical Caries Removal Using Papain-based Enzyme Versus Conventional Rotary Tools in Occlusal Carious Lesions

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

This study will be conducted to assess the efficacy of caries excavation using the papain-based chemo-mechanical method (Brix 3000) in comparison to conventional rotary tools in the reduction of the bacterial population in occlusal carious cavities

NCT ID: NCT03408457 Completed - Clinical trials for Surgical Wound Infection

Influence of Perioperative Fluid Balance on Serum Concentrations of Antibiotics and Surgical Site Infections

Start date: March 14, 2018
Phase:
Study type: Observational

This study evaluates antibiotic serum concentrations in correlation with perioperative fluid balance. Patients will be recruited in rectum and esophageal surgery (representative for low blood loss and restrictive fluid management) and in liver surgery (representative for high blood loss and liberal fluid management). The hypothesis is that high blood loss and liberal fluid management dilute antibiotic serum concentrations thereby potentially increasing surgical site infections.

NCT ID: NCT03406520 Completed - Clinical trials for Peritoneal Dialysis Catheter Exit Site Infection

Chlorhexidine Disk for Prevention of Exit-site Infection in Peritoneal Dialysis Patients

Start date: March 7, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the efficacy and safety of chlorhexidine-impregnated disk in preventing catheter exit-site infection in peritoneal dialysis patients