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NCT ID: NCT00656708 Completed - Burns Clinical Trials

Kerlix Gauze Study in a Burn Trauma Unit and Its Effect on Healthcare Associated Infections in Burn Patients

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Kerlix AMD gauze will decrease the incidence of healthcare associated infections in burn patients. Kerlix AMD gauze will be applied to all patients with open wounds admitted to the burn unit during the prospective portion of the study. All consenting patients will be assessed for hospital associated infections and outcomes. We hypothesis that burn patients will have a decreased number of hospital associated infections compared to historical controls.

NCT ID: NCT00651131 Terminated - Wound Infections Clinical Trials

Cubicin(R) for Complicated Post-surgical Wound Infections

PSW
Start date: June 1, 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to describe the clinical efficacy of CUBICIN therapy in patients with superficial and deep post-surgical Gram-positive wound infections

NCT ID: NCT00651066 Completed - HIV Infections Clinical Trials

Pharmacokinetics of Rifabutin Combined With Antiretroviral Therapy in Patients With TB/HIV Co-infection in Vietnam

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The overall aim of the project is to evaluate rifabutin (RBT) as a replacement for rifampicin (RMP), for the combined treatment of tuberculosis and HIV infection. RBT represents an alternative to RMP for HIV infected patients as its half-life is longer and the enzymatic induction effect appears to be less important on the associated antiretroviral therapy (ART) drugs. This phase II trial is to determine precisely the pharmacokinetics parameters of RBT in combination with different ART regimens in Vietnamese HIV infected patients with pulmonary tuberculosis, in order to define optimal doses that will be further tested in a larger phase III trial comparing safety, tolerability and efficacy of RBT and RMP regimens.

NCT ID: NCT00646958 Completed - Abscess Clinical Trials

Safety and Efficacy Study of Oxazolidinones to Treat Uncomplicated Skin Infections

Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and tolerability of RX-1741, an oxazolidinone, versus linezolid, another oxazolidinone, in the treatment of uncomplicated skin and skin structure infections

NCT ID: NCT00642707 Completed - HIV Infections Clinical Trials

Study of PRO 140 by Subcutaneous Administration in Adult Subjects With HIV -1 Infection

Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is: 1. To assess the antiviral activity of PRO 140 2. To assess the safety and tolerability of PRO 140 3. To generate additional PK, PD and safety data of PRO 140

NCT ID: NCT00642070 Completed - Clinical trials for Urinary Tract Infection

Host Response to Urinary Tract Infection in Women

Start date: February 2008
Phase: N/A
Study type: Observational

This study is being done to identify those elements of the immune response that may predispose a woman to recurrent urinary tract infection. We suspect that lesser effectiveness of certain components of the host response will lead to recurrent urinary tract infection. We will also evaluate the role that the bladder reservoir may play in recurrent urinary tract infection.

NCT ID: NCT00641641 Completed - HIV Infection Clinical Trials

The Effect of Raltegravir on HIV Decay During Primary and Chronic Infection

PINT
Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to measure the decay characteristics of HIV in the blood of patients after taking a combination of anti-HIV drugs, which includes a new class of anti-HIV drug, an integrase inhibitor. This study explores how this new combination of therapy reduces virus in various compartments of the body and immune system.

NCT ID: NCT00640887 Completed - HIV Infections Clinical Trials

Pharmacokinetics of Rifabutin Combined With Antiretroviral Therapy in Patients With TB/HIV Co-infection in South Africa

Start date: February 2009
Phase: Phase 2
Study type: Interventional

The overall aim of the project is to evaluate rifabutin (RBT) as a replacement for rifampicin (RMP), for the combined treatment of tuberculosis and HIV infection. RBT represents an alternative to RMP for HIV infected patients as its half-life is longer and the enzymatic induction effect appears to be less important on the associated antiretroviral therapy (ART) drugs. This phase II trial is to determine precisely the pharmacokinetics parameters of RBT in combination with different ART regimens in Vietnamese HIV infected patients with pulmonary tuberculosis, in order to define optimal doses that will be further tested in a larger phase III trial comparing safety, tolerability and efficacy of RBT and RMP regimens.

NCT ID: NCT00639197 Recruiting - Infection Clinical Trials

UGIST: Ultrasound Guided Internal Jugular Short-Term Central Venous Catheters Tunneling

UGIST
Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if tunneling standard short-term central lines for a short distance under the skin, with the assistance of ultrasound imaging, reduces the risk of central line infections for catheters placed in the neck vein. Previous work has shown that these lines can be tunneled without ultrasound guidance. We wish to determine if the use of ultrasound makes the tunneling procedure safer and easier.

NCT ID: NCT00638677 Completed - Dental Caries Clinical Trials

Bifidobacterium Lactis BB12 and Xylitol Delivered With a Novel Slow-release Pacifier

Start date: June 2004
Phase: Phase 4
Study type: Interventional

Aims: 1. To develop a food supplement containing a health-promoting probiotic bacteria (B. lactis BB12) and xylitol to be administered with a novel soft, possibly occlusion-friendly pacifier. 2. Test in a clinical study how feasible the method is and to study how the intervention affects caries occurrence. Main hypothesis: The administration of B. lactis BB12 and xylitol affects beneficially the dental health of the child.