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Infection clinical trials

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NCT ID: NCT00608738 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Using Whole-Person-Care Guide in Patients Receiving Care for Cancer or Complications From Cancer Treatment

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

RATIONALE: Gathering information about patients with cancer and cancer-related conditions may help doctors learn more about a patient's needs and help doctors plan the best treatment. PURPOSE: This clinical trial is studying how well a whole-person-care guide works in identifying patient needs in patients with cancer or complications from cancer treatment.

NCT ID: NCT00607659 Completed - Clinical trials for CHLAMYDIA INFECTIONS

Immunopathogenesis of Chlamydia

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

Sexually transmitted Chlamydia trachomatis infections are a widespread public health concern due to their prevalence and potentially devastating reproductive consequences, including pelvic inflammatory disease, infertility, and ectopic pregnancy. The goal of this study is to evaluate the risk factors for adverse outcomes following genital tract infection with Chlamydia trachomatis and to evaluate whether or not the presence of C. trachomatis in the rectum act as a reservoir for infection.

NCT ID: NCT00606528 Completed - Clinical trials for Chronic Hepatitis C Virus Infection

FGL2/Fibroleukin and Hepatitis C Virus Infection: A Predictor of Response to Antiviral Therapy

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

The main objective of this study is to assess whether a recently-developed bioassay for the protein FGL2 can be used to predict the progression and/or response to treatment of Hepatitis C Virus disease in patients with chronic HCV infection. The hypothesis is that increased levels of FGL2 and increased numbers of T regulatory cells are associated with a failure to respond to treatment.

NCT ID: NCT00603603 Completed - Clinical trials for Surgical Wound Infection

Controlled Clinical Trial of Supplemental Oxygen for the Prevention of Post-Cesarean Infectious Morbidity

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

Previous studies have demonstrated that patients who undergo surgery while they under general anesthesia have fewer wound infections if they receive higher concentrations of oxygen but this has never been studied in women who are undergoing cesarean section. We plan to randomize women who are undergoing cesarean to receive either standard of care oxygen flow through a nasal cannula during their cesarean section only or a higher concentration of oxygen than they would typically receive through a face mask. Women will receive this therapy during their cesarean and for 2 hours afterwards. We will follow them after their surgery for evidence of infection either in their wound or their uterus.

NCT ID: NCT00602498 Completed - Infection Clinical Trials

Bioequivalency Study of Clarithromycin Tablets Under Fed Conditions

Start date: March 2003
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a potential generic 500 mg clarithromycin tablet formulation compared with Abbott Laboratories 500 mg clarithromycin tablet, Biaxin® following a single 500 mg dose, administered with food.

NCT ID: NCT00601315 Completed - Infection Clinical Trials

Bioequivalency Study of Clarithromycin Tablets Under Fasting Conditions

Start date: April 2003
Phase: N/A
Study type: Interventional

The objective of this study was the bioequivalence of a potential generic 250 mg clarithromycin tablet formulation compared with Abbott Laboratories 250 mg clarithromycin tablet, Biaxin® following a single 250 mg dose, administered in the fasted state.

NCT ID: NCT00599417 Completed - Clinical trials for Respiratory Tract Infections

PulmonarOM (Bacterial Lysates) in Respiratory Tract Infections

Start date: December 2007
Phase: Phase 4
Study type: Interventional

Primary - To evaluate the efficacy of Pulmonaron in the decrease of interleukin-4/interferon gamma after second period of treatment Secondary - To evaluate the efficacy of Pulmonarom in the prevention of upper respiratory tract infections symptoms through patient evaluation of fever or respiratory presence after second period of treatment - To evaluate loss of working or study days after second period of treatment - To evaluate the safety and tolerability of Pulmonarom in the population under study

NCT ID: NCT00599261 Completed - Infection Clinical Trials

MAKE IT CLEAN, Impact of Pocket Revision on the Rate of Infection and Other Complications in Patients Requiring Pocket Manipulation for Generator Replacement and/or Lead Replacement or Revision: A Prospective Randomized Study

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

To determine the effect of scar tissue removal on the rate of infection and any other complications such as bleeding in patients with an ICD or pacemaker who have the device generator or leads replaced or repositioned.

NCT ID: NCT00599053 Terminated - Clinical trials for Respiratory Tract Infections

Early Versus Expectant Treatment of Ureaplasma Infection in Very Low Birth Weight Neonates

Start date: May 2007
Phase: Phase 1/Phase 2
Study type: Interventional

Our hypothesis is that treatment of known Ureaplasma spp. infection of the airways in very low birth weight (VLBW) infants with azithromycin will eradicate the organisms and lessen the proinflammatory state caused by infection that puts them at risk for BPD. We propose to conduct a randomized trial of early (less than 3 days of age) treatment with intravenous azithromycin versus expectant management for VLBW infants with Ureaplasma spp. respiratory tract infection with the following specific aims: (1) Determine microbiological efficacy, pharmacokinetics, and safety of azithromycin treatment for eradication of Ureaplasma spp. in preterm infants, (2) Determine the respiratory outcomes of infants in the two treatment groups and those without respiratory tract Ureaplasma spp. infection

NCT ID: NCT00597090 Completed - Infections Clinical Trials

The Role of Genetic Polymorphisms in Innate Immune Response Genes in Susceptibility to Infections

Start date: February 2003
Phase: N/A
Study type: Observational

The purpose of this study is to better understand genetic susceptibility to infections and the interactions of specific genetic polymorphisms of innate immune receptors with microbial and fungal organisms. The goals of this study are: 1. Find out if some people are more likely to get severe infections, than others. To do this we will compare patients with leukemia who develop severe infections to patients who do not develop infections. 2. Find out if some people are more likely to develop lymphoma than others. To do this we will compare patients with lymphoma to people without lymphoma who are of the same sex and similar age and ethnic background to the patients with lymphoma.