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Acute Respiratory Infection clinical trials

View clinical trials related to Acute Respiratory Infection.

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NCT ID: NCT02943551 Active, not recruiting - Respiratory Disease Clinical Trials

Dialogue Around Respiratory Illness Treatment

DART
Start date: July 18, 2016
Phase: N/A
Study type: Interventional

Unwarranted use of antibiotics for pediatric acute respiratory tract infections (ARTIs) and use of second-line, broad spectrum antibiotics for bacterial ARTIs has contributed to the rapid development of resistance in many strains of bacteria. Provider-parent communication during pediatric visits for ARTIs strongly influence antibiotic prescribing rates. The overall goal of this study is to develop and test a distance learning quality improvement (QI) program called Dialogue Around Respiratory Illness Treatment - DART. The DART program aims to improve provider communication practices and treatment decisions during pediatric ARTI visits, with the ultimate goal being to decrease rates of antibiotic prescribing for these illnesses in children.

NCT ID: NCT02868541 Completed - Clinical trials for Acute Respiratory Infection

Assessment of Pharyngeal Carriage of Microorganisms Responsible for Transmissible Acute Respiratory Infections in HAJJ Pilgrims.

EMIRATH
Start date: January 25, 2017
Phase:
Study type: Observational

The objective of this project is to study the prevalence of viruses and bacteria responsible for transmissible acute respiratory infections in the respiratory tract of pilgrims returning from the trip. The patients included, will be the consultant pilgrims to the traveler health center, and before leaving for Hajj. Based on the results obtained in previous studies, it is estimated that 200 pilgrims will be included each year, 600 in total (inclusion period of 3 years). Respiratory secretions are then collected by nasal swab and throat (swab) prior to departure for the hajj. In return, patients will be reconvened systematic consultation to record medical events potentially encountered during the trip, and it will again be performed the same nasal swabs and throat. It will then be performed on these samples' return from hajj "molecular detection (PCR and RT-PCR) of 35 viruses and bacteria respiratory tropism: influenza (3), RSV (2), metapneumovirus (1), Coronavirus (4), Parainfluenzavirus (4), enteroviruses (4), rhinovirus (1), adenovirus (6) bocavirus, polyomavirus (2), pneumococcus, Bordetella pertussis, Mycoplasma pneumoniae, Chlamydophila pneumoniae, Haemophilus influenzae, Neisseria meningitidis and Coxiella burnetii. Samples "return of hajj" positive should be cultured for the isolation of the strain. For patients positive return, it will be done further research of these 35 viruses and bacteria on samples "start of hajj," the same method described above. In addition to this systematic consultation, and if symptoms return, the pilgrims will be seen in consultation for a diagnosis evaluation and therapeutic management. This study will shed light on the acquisition of microorganisms respiratory tropism during the stay and on the potential risks associated with the circulation of these pathogens after the trip.

NCT ID: NCT02047877 Withdrawn - Clinical trials for Acute Respiratory Distress Syndrome

Airway Inflammatory Response During Illness in Children With Respiratory Failure

Start date: July 2017
Phase: N/A
Study type: Observational

The purpose of this study has two major goals: 1) to measure the amount of two specific hormones interleukin (IL)-10 and interleukin (IL)-12p70 in mucous and blood; and 2) compare the hormone levels in two specific areas of the lung called the trachea (upper airway) and the bronchioles (lower airway). The hormones IL-10 and IL-12p70 are cytokines, special hormones cells use to communicate with each other during inflammation or infection. Cytokines can be measured in mucous and blood. The balance of one cytokine compared to another help doctors to understand how people respond differently to infection. Unfortunately, the amount of IL-10 and IL-12p70 is not known in children, especially children with a lung infection. In addition, we do not know if the balance of these cytokines differ in various regions of the lung. We believe the balance of IL-10 and IL-12p70 is similar whether measured in the upper or lower airways.

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: 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.

NCT ID: NCT01693380 Completed - Influenza Clinical Trials

Effectiveness Assessment of Vaccinating Schoolchildren Against Influenza

Xo_Gripe
Start date: May 2009
Phase: Phase 4
Study type: Interventional

Vaccinating schoolchildren against influenza would prevent the disease among non-vaccinated household members.

NCT ID: NCT01654289 Completed - Clinical trials for Acute Respiratory Infection

University of Wisconsin Meditation & Exercise Cold Study

MEPARI-2
Start date: July 2012
Phase: Phase 2
Study type: Interventional

The primary goal of this project is to determine whether behavioral training in mindfulness meditation or moderate intensity sustained exercise will lead to reductions in acute respiratory infection (ARI) illness, such as common cold and influenza like illness. Specifically, this project aims to: 1. Determine whether an 8-week training program in mindfulness meditation, as compared to the control group, will lead to significant reductions in incidence, duration, and severity of ARI illness. 2. Determine whether an 8-week training program in moderate intensity sustained exercise, as compared to the control group, will lead to reductions in incidence, duration, and severity of ARI illness. 3. Assess whether any observed reductions in ARI illness are accompanied by fewer ARI-related health care visits and less time lost to productive work (reduced absenteeism). 4. Compare the potential benefits of mindfulness meditation to those from moderate intensity sustained exercise. 5. Discern potential mediating factors and causal pathways that might help explain how these interventions lead to improved ARI illness-related outcomes. The investigators' preliminary findings suggest substantial benefit of these interventions in terms of reduced incidence, duration and severity of ARI illness, with corresponding reductions in days of work lost to illness. If the proposed research confirms these findings, there will be major implications for public and private health-related policy and practice, as well as for scientific knowledge regarding health maintenance and disease prevention.

NCT ID: NCT01488435 Completed - Clinical trials for Acute Respiratory Infection

Efficacy and Tolerance of a Follow-On Formula Fed to Children From 36-48 Months of Age

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose is to determine if the consumption of study product has an effect on acute respiratory infections and/or diarrheal disease.

NCT ID: NCT01431469 Completed - Clinical trials for Acute Respiratory Infection

Efficacy and Tolerance of a Follow-On Formula Fed to Children From 12-48 Months of Age in Salvador, Bahia, Brazil

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose is to determine if the consumption of study product has an effect on acute respiratory infections and/or diarrheal disease.

NCT ID: NCT01286285 Enrolling by invitation - Influenza Clinical Trials

Surveillance of Influenza in Paediatric Intensive Care Units in Bavaria

Start date: October 2010
Phase: N/A
Study type: Observational

The purpose of the study is to assess the number of severe, laboratory-confirmed influenza in children hospitalized to paediatric intensive care units. Furthermore, the proportion of these children from all children hospitalized to paediatric intensive care units with acute respiratory infections will be established.