Clinical Trials Logo

Pneumonia clinical trials

View clinical trials related to Pneumonia.

Filter by:

NCT ID: NCT00307528 Completed - Clinical trials for Prophylaxis Invasive Pneumococcal Diseases and Pneumonia

Safety and Efficacy Study of Investigational Pneumococcal Vaccine in Elderly Population

Start date: January 20, 2004
Phase: Phase 2
Study type: Interventional

As the licensed Pneumovax 23™ vaccine is not always satisfactory in elderly subjects, the safety and the immune response of the new investigational pneumococcal protein vaccine is evaluated in healthy elderly population.

NCT ID: NCT00307008 Completed - Clinical trials for Streptococcus Pneumoniae Vaccines

Study to Evaluate the Response Rate to the Licensed Pneumovax 23™ in Elderly Population.

Start date: October 2003
Phase: Phase 2
Study type: Interventional

Streptococcus pneumoniae are bacteria which normally live in the upper respiratory tract of humans. However, these bacteria can also cause severe infectious diseases such as pneumonia, septicemia and meningitis. Elderly subjects are especially vulnerable to these infections, and the diseases can result in death. The currently available licensed Streptococcus pneumoniae vaccine is recommended for prevention of pneumococcal diseases in individuals over the age of 65. However, the antibody level elicited by this vaccine, is not always satisfactory in elderly people. To overcome the problem, GlaxoSmithKline Biologicals is currently developing candidate vaccines that are hoped to work better than the currently available vaccines. As a first step in this development, the present study is being conducted in order to evaluate the immune response to the currently marketed vaccine.

NCT ID: NCT00304395 Completed - Pneumonia Clinical Trials

Pulmonary Infections Masquerading as Community-Acquired Pneumonia

Start date: January 2004
Phase:
Study type: Observational

The purpose of this research is to identify cases from patients who have been referred for consultation to the Infectious Disease Section at the VAMC, Houston, and to compare them with other cases of CAP in order to determine whether there are features that might enable non-CAP cases to be distinguished from CAP.

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: NCT00297674 Completed - Sepsis Clinical Trials

Intravenous Clarithromycin in Septic Syndrome

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

The aim of this clinical trial is to clarify the clinical efficacy of clarithromycin as immunotherapy for the management of septic syndrome by ventilator-associated pneumonia.

NCT ID: NCT00273676 Completed - Clinical trials for Severe Communtity-Acquired Pneumonia

Study on Costs and Safety of Early Conversion From Intravenous to Oral Antibiotic Treatment in Patients With Severe Community-Acquired Pneumonia

Start date: July 2000
Phase: Phase 4
Study type: Interventional

Patients with severe community-acquired pneumonia are included Half of the patients are treated with a 3 day course of intravenous antibiotics, followed, when clinical stable, by a course of oral antibiotics. Efficacy of this treatment is compared to a standard course of 7 days of intravenous antibiotics, which treatment is assigned to the other half of patients. Outcomes measured are clinical cure and costs.

NCT ID: NCT00273325 Completed - Clinical trials for Pneumococcal Infections

Immunogenicity of PCV-7 Vaccine in VLBW Infants

PCV-7
Start date: July 2004
Phase:
Study type: Observational

Premature infants are at a high risk for pneumonia. The PCV-7 vaccine effectively prevents the invasive disease from Streptococcus pneumoniae in full-term infants, but was not thoroughly studied in premature infants. This study evaluated the effectiveness and safety of the vaccine given in routine practice to very low birth weight infants, looking at blood antibody levels 4-6 weeks after the final vaccine dose, and adverse events, survival, infections, and neurodevelopmental outcomes at 18-22 months corrected age.

NCT ID: NCT00272116 Completed - Pneumonia Clinical Trials

Effect of Zinc and Vitamin A Supplementation on Diarrhea, Physical Growth and Immune Response in Malnourished Children

Start date: February 1998
Phase: N/A
Study type: Interventional

Zinc deficiency is common in developing country children, as food intakes are often low, foods from animal sources are infrequently used, the bioavailability of zinc from staple cereal-based diets is limited and zinc losses occur during recurring diarrheal illnesses. Zinc deficiency is associated with impairment in immunological and other defenses against infection and increased rates of serious infections. Due to limitations in currently used biochemical markers, supplementation trials in populations likely to be deficient provide a reliable means of assessing health consequences of zinc deficiency. A significantly lower incidence and prevalence of diarrhea has been observed in zinc supplemented developing country children in several placebo-controlled trials. The effect of routine zinc supplementation on lower respiratory tract infection is still unclear. We, therefore, evaluated the impact of daily zinc supplementation in a representative sample of children aged 6 to 30 months enrolled from a New Delhi slum area, with a sample size sufficient to determine the impact on the incidence of severe diarrhea and acute lower respiratory infection.

NCT ID: NCT00269542 Completed - Pneumonia Clinical Trials

Impact of Zinc Supplementation on Mortality and Hospitalizations in Children Aged 1 Months to 23 Months

Start date: February 2002
Phase: N/A
Study type: Interventional

Children, aged 1 months to 23 months, in the intervention households received zinc, iron and folic acid and those in the control households were administered iron and folic acid (IFA) alone for a period of one year. The primary outcomes were hospitalizations and deaths during this period.

NCT ID: NCT00258661 Completed - Pneumonia Clinical Trials

Is Osteopathic Manipulative Treatment (OMT) Beneficial for Elderly Patients Hospitalized With Pneumonia?

MOPSE
Start date: March 2004
Phase: N/A
Study type: Interventional

Osteopathic Manipulative Treatment (OMT) were used in the 1800s and 1900s to treat pneumonia before the introduction of antibiotics in the mid-1900s. The purpose of this study is to determine if OMT, when used in conjunction with antibiotics and other usual care, will improve the recovery of elderly pneumonia patients.