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Infection clinical trials

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NCT ID: NCT00330902 Completed - Clinical trials for Plasmodium Infections

Randomized Trial of Two Antimalarial Treatments for Clearing Low Density P.Falciparum Parasitaemia in Sudan

Start date: January 2004
Phase: Phase 3
Study type: Interventional

In areas of seasonal malaria transmission, treatment of carriers of malaria parasites, whose parasitaemia persists at very low levels throughout the dry season, could be a useful strategy for malaria control in areas with a short transmission season. We did a randomized trial to compare two regimens for clearance of low level parasitaemia in the dry season.

NCT ID: NCT00324324 Terminated - Breast Cancer Clinical Trials

Moxifloxacin in Preventing Bacterial Infections in Patients Who Have Undergone Donor Stem Cell Transplant

Start date: May 2006
Phase: Phase 3
Study type: Interventional

RATIONALE: A donor stem cell transplant can lower the body's immune system, making it difficult to fight off infection. Giving antibiotics, such as moxifloxacin, may help prevent bacterial infections in patients who have recently undergone donor stem cell transplant. It is not yet known whether moxifloxacin is more effective than a placebo in preventing bacterial infections in patients who have recently undergone donor stem cell transplant. PURPOSE: This randomized phase III trial is studying moxifloxacin to see how well it works compared with a placebo in preventing bacterial infections in patients who have recently undergone donor stem cell transplant.

NCT ID: NCT00324103 Completed - HIV Infection Clinical Trials

Structured Treatment Interruptions in Chronic HIV Infection

Start date: June 2001
Phase: Phase 3
Study type: Interventional

In the last years Structured Treatment Interruptions (STI) have been proposed to reduce HAART-related toxicity and to increase patients’ compliance. ISS PART is a randomized comparison of repeated STIs versus continuous HAART in chronically HIV-infected subjects with persistent suppression of viral replication. The two arms of the study will be compared in terms of immunological response (proportion of patients with CD4>500/mmc) at 2 years.

NCT ID: NCT00323544 Completed - HIV Infections Clinical Trials

SWEET: Once Daily Truvada Versus Twice Daily Combivir for the Treatment of HIV Infection

Start date: October 2004
Phase: Phase 3
Study type: Interventional

This study will investigate whether the simplified regimen of a once daily fixed dose combination of Truvada (emtricitabine and tenofovir disoproxil fumarate [DF]) will be associated with a reduced rate of adverse events, seen with long term use of antiretrovirals, as well as improved adherence compared to a twice daily fixed dose combination of Combivir.

NCT ID: NCT00323453 Completed - Appendicitis Clinical Trials

Wound Infection Alexis Wound Retractor

Start date: March 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the incidence of surgical site wound infection will be reduced in open appendectomy patients through the use of the Alexis® wound retractor.

NCT ID: NCT00321165 Completed - Sepsis Clinical Trials

The AOT (Acridine Orange and Taurolidine) Trial

Start date: June 2006
Phase: Phase 3
Study type: Interventional

Total parenteral (intravenous) nutrition in the home setting (Home TPN or HPN) is a life saving strategy in patients who suffer from severe intestinal failure. Unfortunately, this treatment modality remains complicated by the development of frequent infectious complications. This especially relates to the device that is used to establish venous access, mostly a catheter (Hickman-Broviac type) or a port-a-cath. Taurolodine is an antimicrobial agent without any known side effects or resistance-related problems that holds promise as an effective antibiotic lock solution to prevent catheter infections, as demonstrated recently in a pilot study in HPN patients [Jurewitsch, 2005]. In addition, recently a test has been described which may enable to confirm a suspected diagnosis of central line infection within one hour, the so-called Acridine Orange Leukocyte Cytospin test (AOLC) [Bong, 2003]. For this test, blood that is drawn from the central line is stained with the fluorescent dye acridine orange. Next, microscopic evaluation for the presence of micro-organisms takes place. Implementation of this test might enable to start treatment of the infection and prevent unnecessary removal of non-infected central lines without the necessity to several days wait for culture results.

NCT ID: NCT00318591 Completed - Clinical trials for Urinary Tract Infections

Comparative Study of Intermittent Catheters and Occurrence of Urinary Tract Infections

Start date: April 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the frequency of urinary tract infections with symptoms in spinal cord injured patients requiring intermittent catheterization for emptying the bladder. Patients will use either a coated catheter or an uncoated catheter with gel.

NCT ID: NCT00316043 Completed - Clinical trials for Urinary Tract Infections

Prevention of Renal Failure in Children With Urinary Tract Infections

Start date: May 2006
Phase: N/A
Study type: Interventional

The aim of the study is to describe the current clinical management of young children with urinary tract infections in Dutch primary care and also to describe the possibilities for improvement and potential cost-efficiency of improved care in the light of preventing renal failure.

NCT ID: NCT00315822 Terminated - Clinical trials for Surgical Wound Infection

Supplemental Postoperative Oxygen and Wound Infection in Morbidly Obese Patients

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The investigators propose to test the hypothesis that the incidence of major complications related to infection or inadequate healing is reduced in morbidly obese patients given 80% inspired oxygen during, and for 12-18 hours after, surgery compared with patients given 80% oxygen only during surgery. The primary outcome will be a composite of major complications plausibly related to infection or healing.

NCT ID: NCT00312468 Completed - HIV Infections Clinical Trials

Examining the Link Between Heart Disease and HIV Infection in Women

Start date: October 2006
Phase:
Study type: Observational

Recent studies have shown that HIV infected individuals have an increased risk of developing heart disease, but the reason for this is not fully understood. This study will examine ultrasound test results of blood vessels and laboratory data of HIV infected and HIV uninfected women to examine the link between heart disease and HIV infection.