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Communicable Diseases clinical trials

View clinical trials related to Communicable Diseases.

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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: 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: NCT00312286 Terminated - Clinical trials for Papillomavirus Infections

Efficacy of 851B Gel for Treating High-Risk Cervical Human Papillomavirus Infection in Women.

Start date: April 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate efficacy of 851B gel over a range of concentrations and dosing regimens on high-risk cervical human papillomavirus infection in women.

NCT ID: NCT00305227 Completed - Clinical trials for Urinary Tract Infection

Intravaginal LACTIN-V for Prevention of Recurrent Urinary Tract Infection

Start date: March 2006
Phase: Phase 2
Study type: Interventional

Recurrent urinary tract infections (RUTIS) continue to be a major health problem in women and are now complicated by increasing antibiotic resistance. New preventive approaches are needed. Because most women with RUTI lack the normal protective Lactobacillus (LB) in their vaginal flora, we hypothesized that restoration of LB would reduce RUTIS. In this trail, women with recent UTI are randomized to receive either LB or placebo vaginal capsules and are followed for side effects, for colonization with LB and for occurrence of RUTI over hte next four months.

NCT ID: NCT00304382 Completed - Pneumonia Clinical Trials

Humoral Determinants of Immunity to Pneumococcal Infection

Start date: January 1, 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether there are differences in the level of antibody to capsular polysaccharides of S. pneumoniae or the physiological activity of such antibody after vaccinating patients who have recovered from pneumococcal pneumonia with pneumococcal polysaccharide vaccine (Pneumovax) or conjugate pneumococcal vaccine (Prevnar).

NCT ID: NCT00303589 Completed - Clinical trials for Soft Tissue Infections

A Study of Beta-Lactam in Hospitalized Patients With Skin and Skin Structure Infections

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This 3 arm study will compare the efficacy and safety of beta-lactam with that of 'standard care' in patients with complicated skin and skin structure infections requiring hospitalization. Patients will be randomized to receive 1)beta-lactam 750mg iv q8h 2)beta-lactam 1500mg iv q8h or 3)'standard care' [PRP (nafcillin or flucloxacillin) or vancomycin, plus aztreonam or ciprofloxacin]. The anticipated time on study treatment is <3 months and the target sample size is 100-500 individuals.

NCT ID: NCT00302640 Completed - Rotavirus Infection Clinical Trials

Study of Nitazoxanide Suspension in the Treatment of Diarrhea Caused by Enteric Viruses in Children

Start date: February 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the effect of nitazoxanide suspension in treating diarrhea caused by enteric viruses in children less than 12 years of age.

NCT ID: NCT00300560 Recruiting - Infections Clinical Trials

Efficacy and Safety of Colistin for Therapy of Infections Caused by ESBL Producing K.Pneumoniae or E.Coli

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

In patients with documented ESBL-producing E.coli and Klebsiella pneumoniae will be allocated to receive colistin or conventional antibiotic regimen.

NCT ID: NCT00299663 Completed - Clinical trials for Streptococcal Infections

Long Term Follow-up of Patients With Group A Streptococcal Infection Originating From the Genital Tract

Start date: February 2006
Phase: N/A
Study type: Observational

Group A streptococcus (GAS) causes a variety of human infections. It is also an uncommon but serious cause of postpartum infections. In contrast to group B streptococcus (GBS) infection, which causes illness and death in newborns disproportionately more often than it does in mothers, perinatal GAS infection primarily affects mothers . Invasive GAS infection is defined by the isolation of GAS from a normally sterile site (e.g., blood) or by the isolation of GAS from a nonsterile site in the presence of the streptococcal toxic shock syndrome or necrotizing fasciitis. A postpartum case of invasive GAS is defined as isolation of GAS during the postpartum period, in association with a clinical postpartum infection (e.g., endometritis) or from either a sterile site or a wound infection. Because of the burden and severity of invasive GAS infection, the Centers for Disease Control and Prevention (CDC) hosted a meeting in to formulate guidelines for responding to postpartum and postsurgical GAS infections. However, we could not find any recommendations for long-term follow-up of patients who had GAS infection subsequent to delivery or gynaecological procedures, or further recommendations regarding subsequent delivery or gynaecological invasive procedures. It is possible that women who had GAS as a cause of vaginal infection may have a tendency to be carriers of this organism, but this has never been proven. We believe it is of importance to determine if women who have had one infection may be long-term carriers which may pose a risk during future pregnancies. The objective of the present study is to evaluate the incidence of long term gynaecological carrier state of patients who had GAS invasive infection following delivery, and to provide guidelines for follow-up and treatment of such patients. The proposed study may answer the question whether this endogenous GAS origin represents chronic GAS carrier state, similar to the known GBS carrier state. As some of these patients had severe infections (sometimes life threatening) a protocol for long-term follow up and management is necessary in case an invasive procedure is done (IUD insertion, endometrial biopsy, curettage or delivery) in order to prevent recurrent infection. The information collected in the study will enable us to afford recommendations for follow up and prophylaxis in the future.