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Bacterial Infections clinical trials

View clinical trials related to Bacterial Infections.

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NCT ID: NCT02544230 Completed - Sepsis Clinical Trials

Granulocyte Transfusions in Hematological Patients With Febrile Neutropenia

Start date: January 2004
Phase: N/A
Study type: Observational

The investigators retrospectively evaluated the efficacy of granulocyte transfusions as adjunctive treatment for severe infections in neutropenic fever unresponsive to antimicrobial therapy in hematological patients.

NCT ID: NCT02543827 Completed - Clinical trials for Urinary Tract Infection Bacterial

Evaluation of the Efficacy and Safety of MV140

MV140
Start date: November 2015
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy and safety of a biological vaccine (MV140) in women with Recurrent Urinary Tract Infections (RUTI) compared with a placebo group.

NCT ID: NCT02541695 Completed - Diarrhea Clinical Trials

Characterization of Resistance Against Live-attenuated Diarrhoeagenic E. Coli

CORAL
Start date: September 2015
Phase: N/A
Study type: Interventional

Although the existing diarrhoeagenic Escherichia coli (E. coli) challenge model is already suitable for dietary interventions in its current form, further characterization of the working-mechanism of the attenuated strain and further optimization of the study design will enable the investigators to better select those ingredients that affect the key pathophysiological processes. The aim of the CORAL study is to further characterize and increase the discriminative power of the diarrhoeagenic E. coli challenge model.

NCT ID: NCT02500654 Completed - Inflammation Clinical Trials

Regenerative Surgical Treatment of Peri-implantitis

Start date: December 2008
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate if surgical treatment of peri-implantitis with enamel matrix derivative (Emdogain®, EMD) will have an additional effect on the healing outcome, changes in the peri-implant microflora and on the inflammatory response in the periimplant pocket at 12 months.

NCT ID: NCT02475876 Completed - Clinical trials for Bacterial Infections

PK of Clindamycin and Trimethoprim-sulfamethoxazole in Infants and Children

PBPK
Start date: November 2015
Phase: Phase 1
Study type: Interventional

Developmental changes in physiology during childhood influence drug dosing. Failure to account for these changes leads to improper dosing, which is associated with decreased drug efficacy and safety in children. Population physiologically-based pharmacokinetic (PBPK) modeling offers the opportunity to predict optimal drug dosing based on physiologic parameters adjusted for developmental changes. PBPK models are mathematical constructs that incorporate physiologic processes with drug characteristics and genetic variances to characterize the dose-exposure relationship across the age continuum. These models integrate drug-specific (e.g., metabolism, protein binding) and systems-specific (e.g., organ size, blood flow) information to predict the effect of different factors (e.g., age, genetic variants, disease) on drug exposure. By accounting for these factors and using data from clinical trials to confirm the modeling, PBPK models can reduce the number of children needed for clinical trials while maximizing dose-based efficacy and safety. This trial will evaluate a platform to prospectively validate population PBPK models in children. The study drugs, clindamycin and Bactrim (aka TMP-SMX), are ideal candidates to evaluate population PBPK models in children due to their differing physico-chemical properties and elimination pathways. In addition, a trial of clindamycin and TMP-SMX has broad clinical applicability, as both drugs are among the most commonly used agents to treat gram-positive infections in infants and children.

NCT ID: NCT02452047 Completed - Clinical trials for Bacterial Infections

Efficacy and Safety of Imipenem+Cilastatin/Relebactam (MK-7655A) Versus Colistimethate Sodium+Imipenem+Cilastatin in Imipenem-Resistant Bacterial Infection (MK-7655A-013)

RESTORE-IMI 1
Start date: August 21, 2015
Phase: Phase 3
Study type: Interventional

The study will evaluate the efficacy and safety of imipenem+cilastatin/relebactam (MK-7655A) versus colistimethate sodium+imipenem+cilastatin in the treatment of imipenem-resistant bacterial infections. Infections evaluated in the study will be hospital-acquired bacterial pneumonia (HABP), ventilator-associated bacterial pneumonia (VABP), complicated intra-abdominal infection (cIAI), and complicated urinary tract infection (cUTI).

NCT ID: NCT02436876 Completed - Bacterial Infection Clinical Trials

Study to Assess Safety and Clinical Activity of Local MBN-101 in Treatment of Infected Bone Sites

Start date: May 24, 2016
Phase: Phase 2
Study type: Interventional

This study evaluates the safety and clinical benefit of MBN-101 administered intraoperatively to osteosynthesis or osteomyelitis sites for patients diagnosed with an orthopedic infection, with or without orthopaedic hardware. Three quarters of the patients will receive MBN-101, while the other one quarter will receive placebo.

NCT ID: NCT02426918 Completed - Clinical trials for Bacterial Infections

Study of Debio 1450 for Bacterial Skin Infections

Start date: May 2015
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of 2 different doses of intravenous and oral Debio 1450 compared with intravenous vancomycin and oral linezolid in the treatment of patients with staphylococcal ABSSSI.

NCT ID: NCT02378480 Completed - Clinical trials for Bacterial Infections

Omadacycline Versus Linezolid for the Treatment of ABSSSI (EudraCT #2013-003644-23)

Start date: June 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of omadacycline as compared to linezolid in the treatment of adults with acute bacterial skin and skin structure infections.

NCT ID: NCT02375477 Completed - Clinical trials for Clostridium Difficile

Improved Adherence to C. Difficile Isolation Protocols Through Improved Education Methods

Start date: January 27, 2015
Phase: N/A
Study type: Interventional

This clinical trial studies how well inter-disciplinary educational methods work in improving adherence to isolation protocols in patients with Clostridium (C.) difficile infections. An inter-disciplinary educational method may help to prevent the spread of infection.