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Infection clinical trials

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NCT ID: NCT02693639 Not yet recruiting - Infection Clinical Trials

Prediction Value of PANX1 in Infection Post Liver Transplantation

Start date: February 2016
Phase: N/A
Study type: Observational

The purpose of this study is to determine prediction value of PANX1 expression in infection post liver transplantation.

NCT ID: NCT02689193 Completed - Fever Clinical Trials

IDIS Project Work Package 2: Establishing a Biobank at ITM and Collaborating Centres

IDIS
Start date: September 2014
Phase:
Study type: Observational

The IDIS study aims to develop a new rapid diagnostic test for invasive salmonellosis using samples (blood, urine) collected from patients with fever and healthy controls at the Institute of Tropical Medicine (ITM) and collaborating centers. The samples are collected after informed consent and/or assent is given by the participant and are stored in a -80 ⁰C freezer after processing (centrifugation and/or aliquoting). Basic information regarding the patient and the samples are coded and stored in a protected Microsoft Access database. The samples will be shipped to Belgium for proteomic analysis. Identification of Salmonella specific proteins in the samples will hopefully support the development of a rapid diagnostic test. Once this test has been developed, the samples will also be used for validation and evaluation of this test.

NCT ID: NCT02688322 Completed - Clinical trials for Acinetobacter Infections

Pharmacodynamics Modeling to Optimize Dosage Regimens of Sulbactam in Patients With Acinetobacter Infections

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

Acinetobacter species have emerged as agents of serious nosocomial infections in critically ill patients. Only a few effective antibiotics are currently available for the treatment of this pathogen and, therefore, sulbactam is being considered as an alternative treatment option. The aims of this study were to i) reveal the population pharmacokinetics and ii) assess the probability of target attainment (PTA) of sulbactam in septic critically ill patients caused by Acinetobacter spp. infections. The study was conducted in septic critically ill patients caused by Acinetobacter spp. Each patient received 2 g every 12 h of sulbactam for 10 days, after which PK studies were carried out on day 4 of sulbactam therapy and a Monte Carlo simulation was performed to determine the probability of attaining a specific pharmacodynamic target.

NCT ID: NCT02688244 Recruiting - Infection Clinical Trials

Irrigation Versus Suction in Complicated Acute Appendicitis

ISAAC
Start date: November 2015
Phase: N/A
Study type: Interventional

This study evaluates the intraabdominal abscess rate after laparoscopic appendectomy in complicated acute appendicitis performing irrigation of the abdominal cavity or only suction without lavage.

NCT ID: NCT02687217 Completed - Wound Infection Clinical Trials

Effect of Peri-operative Supplemental Oxygen in Wound Infection After Appendectomy

Start date: November 2011
Phase: N/A
Study type: Interventional

The study evaluates the role of supplemental hyper-oxygenation given perioperatively on wound site infection after appendectomy. Half of the patients received ≥50% oxygen and half of them received no oxygen during the surgical procedure.

NCT ID: NCT02686645 Not yet recruiting - Clinical trials for Clostridium Difficile Infection

Fecal Microbiota Therapy for Recurrent Clostridium Difficile Infection

Start date: December 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Interventional, single arm, single-centre trial to evaluate the effectiveness and safety of fecal microbiota therapy (FMT) in the investigators population.

NCT ID: NCT02685696 Completed - Clinical trials for Surgical Site Infection

Surgical Site Infection in Caesarean Section Using Alexis O Compared to Metal Retractors

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

Objective: To investigate if the use of the newly designed Alexis O Retractor leads to improved intra-operative and post-operative surgical outcomes in the setting of planned elective Caesarean Sections. Study Design: This ethically approved study is designed as a prospective, randomized controlled trial in planned, first time Caesarean Sections with 200 patients randomized to either the Alexis-O Retractor group or the conventional group. Patients with wound healing problems, connective tissue disorders, insulin dependent diabetes, bleeding disorders, previous major abdominal surgery and chorioamnionitis are excluded. Outcomes include surgical site infection, intraoperative parameters such as tissue damage, postoperative analgesia requirements and patient satisfaction scores.

NCT ID: NCT02683096 Completed - Clinical trials for Cytomegalovirus Infections

Screening for Congenital Cytomegalovirus Infection in Newborns

CMV
Start date: February 2016
Phase:
Study type: Observational

Our central hypothesis is that screening newborn infants who either fail their newborn hearing test or have a diagnosis of small for gestational age (SGA) will lead to better identification of infants with congenital CMV infection and enhanced rates of therapeutic intervention. This has the potential to significantly improve outcomes for infants with this common viral infection. This particular cohort of patients have not been well studied locally or regionally. In addition, in view of current legislation that will be effective in January, 2016 this is a timely project that will provide preliminary data for future statewide recommendations around CMV testing of newborn infants. This will be a pilot/feasibility study to obtain preliminary data for an Illinois Department of Public Health (IDPH) Title V grant. Although not guaranteed, preliminary discussions with the IDPH are highly encouraging giving the statewide interest in this topic.

NCT ID: NCT02681458 Completed - Clinical trials for Skin and Subcutaneous Tissue Fungal Infections

Superficial and Cutaneous Fungal Infections Among Drug-users in Northeast Region of Iran

Start date: August 2013
Phase: N/A
Study type: Observational

The purpose of this study was about survey of prevalence of fungal infections among drug users referring to methadone wards of Hospitals in northeast region of Iran

NCT ID: NCT02681263 Active, not recruiting - Clinical trials for Urinary Tract Infections

Efficacy of Temocillin in Urinary Tract Infection Due to ESBL Producing and AmpC Hyperproducing Enterobacteriaceae

TEMO-ESBL
Start date: April 2016
Phase: Phase 4
Study type: Interventional

The present study aims at demonstrating the efficacy of temocillin in the treatment of UTI requiring parenteral therapy due to a confirmed ESBL producing or AmpC hyperproducing Enterobacteriaceae, resistant to quinolones and Bactrim® in France. In addition, this study will describe and support the use of high dose (6g/day) of temocillin which could be of interest for the treatment urinary tract infection due to multi-resistant bacteria having high MIC (up to 32 mg/L). The investigators will also evaluate the tolerance of the drug by monitoring the adverse event and the incidence of eventual Clostridium difficile associated infection.