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Respiratory Tract Infections clinical trials

View clinical trials related to Respiratory Tract Infections.

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NCT ID: NCT04267952 Completed - Hand Hygiene Clinical Trials

Hand Hygiene Intervention Program on Primary School Students' Health Outcomes and Absenteeism in School

Start date: September 9, 2019
Phase: N/A
Study type: Interventional

The most common infections in schools are acute respiratory infections (colds, pharyngitis, influenza and others) and diarrheal diseases. The incidence of these infections may also be an important cause of school absenteeism, leading to negative outcomes in both education and health. WHO states that handwashing a well-known primary infection control measure, is the most important hygiene measure to prevent the spread of infection when handwashing is done with soap and water. Since behavioral choices that determine lifestyle are made in childhood, it is important that health education in hand hygiene be implemented as early as possible to improve healthy behaviors. In this context, schools are important structures for information and behavior change about water, sanitation and hygiene interventions. Planned Behavior Theory (PBT) states that intention is the main precursor of behavior. According to the theory, intention is guided by three independent variables (perceived behavior control, attitudes and subjective norms), and intention formation leads to the development of behavior. The theory has been used in a study to improve hand hygiene behavior in health workers, but it has not been used in the literature to improve hygiene behaviors in children. Researches indicate that students who do not attend school frequently or for a long time have difficulty in mastering the subject described in the lesson and that school absenteeism is an issue that should be emphasized in education. Therefore, hand hygiene has a simultaneous effect that improves both education and health and contributes to a safe and healthy learning environment. The aim of this research is; To test the effect of hand hygiene intervention program based on Planned Behavior Theory on students' health outcomes and school absenteeism.

NCT ID: NCT04245800 Completed - Clinical trials for Respiratory Tract Infections

Home Testing of Respiratory Illness

Start date: December 13, 2019
Phase:
Study type: Observational

The main goal of this research study is to use data from activity trackers (such as Fitbits), lab tests, and surveys to see if activity, sleep, and heart rate data can tell the difference between when someone has a respiratory illness (e.g., flu) and when they are feeling healthy. The research will also study an investigational flu@home test and app. If successful, results from the study could be used in the future to better identify people with respiratory illness. In addition, this study will test the accuracy of an at-home flu test kit compared to laboratory test results.

NCT ID: NCT04244084 Completed - Clinical trials for Viral Respiratory Infection

Clinical Trial of Efficacy and Safety of ММН-407 in Acute Respiratory Viral Infection

Start date: October 8, 2019
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and safety of ММН-407 in treatment of acute respiratory viral infection (ARVI).

NCT ID: NCT04239521 Completed - Asthma Clinical Trials

The Epidemiology, Management, and the Associated Burden of Related Conditions in Alopecia Areata

Start date: October 1, 2020
Phase:
Study type: Observational

This study series consists of four related studies and aims to explore and describe many important elements of alopecia areata over three key areas: (1) the current epidemiology of alopecia areata, (2) the prevalence and incidence of psychiatric co-morbidities in people with alopecia areata, (3) the prevalence and incidence of autoimmune and atopic conditions in people with alopecia areata, and (4) the incidence of common infections in people with alopecia areata.

NCT ID: NCT04223453 Completed - Clinical trials for Acute Infection Respiratory

Body Composition Measurements in Pneumonia

Start date: January 5, 2019
Phase:
Study type: Observational

The purpose of this study is to validate and standardize bioelectrical impedance analysis (BIA, Maltron BioScan touch i8) for estimating body composition in hospitalized elderly patients with pneumonia. Body composition assessments with BIA and dual-energy x-ray absorptiometry (DXA,

NCT ID: NCT04196101 Completed - Clinical trials for Respiratory Syncytial Virus

A Study to Assess EDP-938 for the Treatment of Acute Upper Respiratory Tract Infection With Respiratory Syncytial Virus in Adult Subjects

RSVP
Start date: January 22, 2020
Phase: Phase 2
Study type: Interventional

This was a randomized, double-blind, placebo-controlled, multicentre, phase 2 study to evaluate the efficacy, safety and tolerability of orally administered EDP-938 in adults with RSV infection.

NCT ID: NCT04174937 Completed - Clinical trials for Infections, Respiratory

PA Tolerability, Safety and Pharmacokinetics in Healthy Volunteers

PA
Start date: June 17, 2016
Phase: Phase 1
Study type: Interventional

This is a first-in-human (FIH) study to explore the safety, tolerability and pharmacokinetics of PA after oral ascending dose administration to healthy male volunteers.

NCT ID: NCT04144491 Completed - Diarrhea Clinical Trials

Effect of L. Rhamnosus Yoba on RTI and Other Health Outcomes Among Children (3-6 Years) in Uganda

Start date: September 16, 2019
Phase: N/A
Study type: Interventional

This is a nutritional trial with two arms: 1) Intervention arm of Probiotic Yoghurt containing Lactobacillus rhamnosus yoba 2012 and 2) Control arm of custard-like dairy product. The study subjects are 200 children between the age of 3-6 years that attend a school in Southwestern Uganda, Sheema district. Children will be randomized and enrolled in either the yoghurt (100 children) or the placebo (100 children) arm. The children will be monitored for 3 weeks in the baseline in regards to the incidence of common childhood diseases. During these three weeks, stool, saliva and urine samples will be collected. Also measurement of anthropometric indicators (weight and height) will take place. Subsequently, the children will consume either 100ml yoghurt or 100ml placebo product, once per day for five days per week for nine weeks, while being daily monitored in regards to the incidence of common childhood diseases. The same samples (stool, urine and saliva) and assessments (anthropometric) will take place at end line.

NCT ID: NCT04139681 Completed - Clinical trials for Respiratory Tract Infection Viral

Safety and Efficacy of the Sore Throat Lozenges to Treat Acute Sore Throats

Start date: March 12, 2019
Phase: Phase 4
Study type: Interventional

Aim of this study is to investigate safety and efficacy of A. Vogel Sore throat lozenges for the treatment of of acute sore throats

NCT ID: NCT04127682 Completed - Clinical trials for Antibiotic Side Effect

Antibiotic Prescription for Children With Acute Upper Respiratory Tract Infections in Assiut District

Start date: January 1, 2021
Phase:
Study type: Observational

Antibiotics are one of the most commonly prescribed drugs in pediatric care all over the world. Over prescription of antibiotics is a major public health problem and the most important factor in the emergence of antibiotic resistance. It is important to study physicians' antibiotic prescribing behavior to understand its determinant and for further planning of appropriate interventions to optimize antibiotic prescription.