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NCT ID: NCT00638170 Completed - Clinical trials for Urinary Tract Infections

Cranberry Juice in the Prevention of Urinary Tract Infections in Children

Start date: May 2001
Phase: N/A
Study type: Interventional

The objective of the study is to determine whether recurrences of urinary tract infection in children can be prevented with cranberry juice.

NCT ID: NCT00637429 Recruiting - HIV Infections Clinical Trials

HIV-HBV Co-Infection and Liver Disease

Start date: November 2007
Phase: N/A
Study type: Observational

Human immunodeficiency virus/Hepatitis B virus (HIV/HBV) co-infections are frequently observed due to shared routes of transmission, with reported figures indicating 6-9% of HIV-infected individuals in developed countries are chronically infected with HBV. HIV infection impacts on the natural progression of HBV infection, increasing levels of HBV replication and the risk of liver-associated mortality. Liver diseases associated with HBV are affected by the antiviral drugs used for HIV infection (toxic side effects), the current immune function in the patient, by improvements in the immune system brought about by control of the HIV infection, and by the development of resistance to the antiviral agents used for both the hepatitis B and the HIV infection. Co-infection with HBV increases the risk for hepatotoxicity in those individuals receiving highly active antiretroviral therapy (HAART) for their HIV infection. This study will recruit patients who are co-infected with HIV and HBV, and are currently taking or who are about to commence HAART. The study cohort will include HIV-HBV co-infected individuals from the Alfred Hospital, the Royal Melbourne Hospital and high case load GP clinics who are referred to the Alfred Hospital. The aim of the study is to investigate chronic hepatitis B and its impact on the progression of liver disease in HIV-infected persons receiving HAART. This will be achieved by 6 monthly assessment with medical history, physical examination, bloods for markers of liver disease and hepatitis B activity and completion of questionnaires to measure adherence and alcohol use.

NCT ID: NCT00634608 Completed - Obesity Clinical Trials

Integrating Targeted MedlinePlus Health Prescriptions Into Clinic Practice Workflow

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

The specific aim of this proposed project is to implement a standard process for integrating MedlinePlus health information prescriptions into the clinic workflow. Hypothesis 1: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more likely to seek information / use MedlinePlus compared with individuals in the control group. Hypothesis 2: Individuals in the intervention group who receive tailored email health information with provider selected MedlinePlus links and added commentary for patient specific conditions will be more satisfied with the information received compared with individuals in the control group.

NCT ID: NCT00633191 Completed - Cystic Fibrosis Clinical Trials

Anti-pseudomonas IgY to Prevent Infections in Cystic Fibrosis

PseudIgY
Start date: November 2003
Phase: Phase 1/Phase 2
Study type: Interventional

Hypothesis: Daily gargling with specific avian antibodies against Pseudomonas aeruginosa will prevent infections with this bacteria in patients with Cystic fibrosis (CF).

NCT ID: NCT00633152 Completed - Bacterial Infection Clinical Trials

Efficacy and Safety of Ceftaroline Versus Linezolid in Subjects With Complicated Skin and Skin Structure Infections

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

The purpose of this study is to determine whether ceftaroline is effective and safe in the treatment of complicated skin and skin structure infections in adults.

NCT ID: NCT00633126 Completed - Infection Clinical Trials

Pharmacokinetics of Ceftaroline in Subjects 12 to 17 Years of Age

Start date: March 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the pharmacokinetics of ceftaroline in pediatric subjects

NCT ID: NCT00632463 Completed - Clinical trials for Upper Respiratory Tract Infection

RI-001 in Immunosuppressed Respiratory Syncytial Virus (RSV) Infected Patients at Risk of Lower Tract RSV Illness

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

RSV infections can develop into serious, life threatening conditions among immunocompromised patients. The objective of this study (ADMA 001) is to evaluate the safety and efficacy of RI-001 for the prevention of lower respiratory tract infections in immunocompromised patients identified as being infected with RSV in the upper respiratory tract.

NCT ID: NCT00630513 Completed - Clinical trials for Intra-Abdominal Infection

T.E.A. Study Three Days Ertapenem Versus Three Days Ampicillin- Sulbactam

TEA
Start date: January 2008
Phase: Phase 4
Study type: Interventional

The aim of the study was to compare the activity (efficacy and safety) of Ertapenem administered according to a short treatment for three days versus a short treatment for three days with AS in patients with an community acquired IAI of mild to moderate severity.

NCT ID: NCT00630162 Completed - HIV Infections Clinical Trials

Intestinal Protozoal Infections and Sexual Transmitted Diseases Among Targeted Cohorts

Start date: March 2007
Phase: N/A
Study type: Observational

In this two-year study, we will target two high risk groups, including MSM of HIV-infected and those of non-HIV-infected. We will avail the serodiagnosis to detect the potential amebic carriers in both groups; and use microscopy to detect protozoas other than amebiasis. Meanwhile we will also survey the patients' status of sexual transmitted diseases (STD). For the amebic carriers, we will apply specific antigen and molecular biologic method to follow up the duration of the persistence of fecal amebas. We try to clarify the dynamic change of amebic carriage.

NCT ID: NCT00627393 Completed - Infection Clinical Trials

Safety and Effectiveness of Granulocyte Transfusions in Resolving Infection in People With Neutropenia (The RING Study)

RING
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Neutropenia, a condition characterized by an abnormally low number of infection-fighting white blood cells called neutrophils, commonly develops in people who have undergone chemotherapy or hematopoietic stem cell (HSC) transplantation. The severely reduced immunity of those with neutropenia can put them at risk of entry of life-threatening infections, making the implementation of treatments that increase white blood cell numbers important. Several studies have shown that the transfusion of donor granulocytes, a type of white blood cell that includes neutrophils, is effective in promoting the recovery of adequate numbers of granulocytes. However, granulocyte transfusions can cause side effects, and it is not known whether the success of the therapy outweighs the health risks of the side effects. This study will evaluate the safety and effectiveness of granulocyte transfusions in treating people with a bacterial or fungal infection during neutropenia.