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Respiratory Tract Infections clinical trials

View clinical trials related to Respiratory Tract Infections.

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NCT ID: NCT01858974 Completed - Pneumonia Clinical Trials

Fast Identification of Pathogen in the Setting of Pneumonia Using Multiplex PCR

Start date: June 2013
Phase: N/A
Study type: Observational

With this study the investigators want to determine, if a fast identification of germs, causing infections of the lower respiratory tract, is possible through the use of Multiplex PCR technology - a method that allows on time detection of bacteria in medical specimen by identifying DNA sequences that are known to be specific for the respective microbe. Therefore aspiration samples from the respiratory tracts of ventilated patients, which are suspected to develop such an infection, will be collected and analyzed by using a multiplex PCR (polymerase chain reaction) application situated on the intensive care unit. The investigators want to determine if Multiplex PCR diagnostic could be a faster alternative to conventional microbiological methods. The results of the Multiplex PCR analyses therefore will be compared with results of conventional microbiological methods.

NCT ID: NCT01843842 Completed - Clinical trials for Acute Upper Respiratory Tract Infections

Clinical Trial of Safety and Clinical Efficacy of Ergoferon in Liquid Dosage Form in Treatment of Acute Upper Respiratory Tract Infections in Children

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is: - to assess safety of the liquid dosage form of Ergoferon for treatment of acute upper respiratory tract infections in children; - to assess clinical efficacy of the liquid dosage form of Ergoferon for treatment acute upper respiratory tract infections in children.

NCT ID: NCT01842997 Completed - Influenza Clinical Trials

Safety of H1N1 Influenza Vaccination in Pregnant Women

Start date: October 2009
Phase: Phase 4
Study type: Interventional

Since October 2009, H1N1 influenza vaccine has developed and approved of immunization in population in China. However, there was little epidemiological evidence of safety when vaccinated in healthy pregnant women. The main objective of this study is to assess the safety of split-virion inactivated H1N1 vaccine without adjuvant when administered in healthy pregnant women. It is a stratified and controlled clinical trial in healthy pregnant women. And participants were included up to 226 healthy pregnant women aged 18 -35 years old who have no history of novel influenza H1N1 infection or novel influenza H1N1 vaccination. The pregnancy week ranged from 5 weeks to 32 weeks. Subjects were divided into 2 groups: vaccinated group(122) and unvaccinated group(104). Subjects in the vaccinated group were administered one dose of 15μg H1N1 vaccine. Subjects in the unvaccinated group received no vaccine as controls. Safety will be measured by assessment of pregnancy outcomes. And observation time for pregnancy outcomes was lasting for 28 days postpartum since vaccinated; and protective effect was observed for six months.

NCT ID: NCT01839474 Completed - Pneumonia Clinical Trials

CPAP Survival Study in Ghana

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of a continuous positive airway pressure (CPAP) machine (a device that blows air into the lungs) decreases the chance of a child dying from difficulty breathing.

NCT ID: NCT01824719 Unknown status - Clinical trials for Acute Tracheobronchitis

A Registry Study on Reduning(a Chinese Medicine Injection)Used in Hospitals in China

Start date: January 2013
Phase: N/A
Study type: Observational [Patient Registry]

This study was advocated by Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences in January 2013. The purpose of this study is to make a event monitoring to see whether Reduning injection is safe and the characteristic and mechanism of anaphylactic reaction used Reduning injection in hospitals in China.

NCT ID: NCT01814293 Withdrawn - Signs and Symptoms Clinical Trials

Comparison of Supportive Therapies for Symptom Relief From Pediatric Upper Respiratory Infections (URIs)

Start date: May 2013
Phase: N/A
Study type: Interventional

This is a nonblinded randomized controlled trial which is a survey-based comparison between supportive treatments for symptom relief from pediatric upper respiratory infection (URI). The primary objective of this study is to determine if the use of handheld humidifier improves URI symptom scores and/or reduces use of over the counter medications compared to other supportive treatments for pediatric URIs (ie. OTC cold medications, room air humidifier). Study duration is approximately 1 year and the individual intervention is 4 days.

NCT ID: NCT01806285 Completed - Clinical trials for Viral Respiratory Infection

Sample Collection to Evaluate an Investigational Instrument for the Detection of Respiratory Viruses in Nasopharyngeal Swabs

Start date: February 2013
Phase: N/A
Study type: Observational

The purpose of this sample collection study is to prospectively collect respiratory viral clinical samples, conduct standard of care comparator testing and archive the collected residual samples for future testing in order to establish the clinical performance characteristics of the investigational instrument.

NCT ID: NCT01800747 Completed - Acute Otitis Media Clinical Trials

Clinical Trial for the Assessment of Delayed Antibiotic Treatment in Pediatric (DAP-Pediatrics)

DAP
Start date: June 2012
Phase: Phase 4
Study type: Interventional

The general hypothesis is that delayed antibiotic treatment strategy present similar effectiveness, when compared with non-prescription of antibiotics or the prescription of antibiotics, in the non-complicated acute respiratory tract infections in pediatric patients.

NCT ID: NCT01794819 Completed - Clinical trials for Respiratory Tract Infections

Usefulness of C-reactive Protein Testing in Acute Cough

Start date: January 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the usefulness in Russian general practice of C-reactive protein testing in patients with acute cough or lower respiratory tract infections. In addition to studying the effect of C-reactive protein testing on the prescription of antibiotics, the purpose is to find out whether the frequency of referral to radiography could be reduced.

NCT ID: NCT01791608 Completed - Diarrhea Clinical Trials

Zinc Sulphate vs. Zinc Amino Acid Chelate

ZAZO
Start date: March 2012
Phase: Phase 4
Study type: Interventional

Acute respiratory infection and acute diarrhea are among the most prevalent diseases of childhood increase the burden of morbidity and mortality in children under 5 years. Among the possible strategies for its prevention is important to count on good nutritional status for use in developing a good immune response to infections. Zinc deficiency has been shown to favor the development of infections and has been considered a real public health problem. Within the zinc compounds used are zinc amino acid chelate and zinc sulphate, the first that has shown evidence of being better absorbed and tolerated. We propose a study showing the effectiveness of zinc amino acid chelate and zinc sulphate in the prevention of acute diarrheal disease and acute respiratory infection.