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Respiratory Tract Infections clinical trials

View clinical trials related to Respiratory Tract Infections.

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NCT ID: NCT01075204 Completed - Clinical trials for Respiratory Tract Infection

Clarithromycin Modified Release Observational Study for Evaluation of Treatment, Tolerability & Recovery Time in Saudi & Egyptian Clinical Settings (CLOSER)

CLOSER
Start date: January 2011
Phase: N/A
Study type: Observational

The objective is to describe the time to recovery of symptoms (cough, mucus, fever, sore throat, and others), tolerability and compliance of treatment with clarithromycin once daily in patients with upper or lower respiratory tract infections in the routine clinical practice.

NCT ID: NCT01073033 Completed - Diarrhea Clinical Trials

Oral Supplement for Pregnant and Lactating Mothers

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

To assess protection against early life infections through supplementation of mothers during pregnancy to the newborns' growth, morbidity, immune status intra and extra-uterine.

NCT ID: NCT01069874 Completed - Influenza Clinical Trials

Trial of Vitamin D Supplementation for the Prevention of Influenza and Other Respiratory Infections (ViDiFlu)

ViDiFlu
Start date: March 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Purpose: The study null hypothesis is that vitamin D supplementation will not influence time to acute respiratory tract infection in sheltered accommodation residents.

NCT ID: NCT01068990 Recruiting - Severe Pneumonia Clinical Trials

Detection and Characterization of Lower Respiratory Infections in Critically Ill Patients

Start date: March 2010
Phase:
Study type: Observational

This study is a prospective observation study for lower respiratory tract infections in medical intensive care unit. Microbiologic and clinical characteristics and outcomes of patients with severe pneumonia in medical intensive care unit will be monitored and analyzed.

NCT ID: NCT01062256 Completed - Infection Clinical Trials

Study of Count Coughs in Subjects With Acute Upper Respiratory Tract Infections

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

The objectives of this study are: a) to assess the feasibility and sensitivity of manually count cough bouts over a 4-hour period; b) to assess the effects of buckwheat honey and guaifenesin 400 mg immediate release tablets compared to placebo on the frequency and severity of acute cough due to upper respiratory tract infection and c) to evaluate the correlation between cough bout frequency and subjective assessments of cough severity. The hypotheses to be tested is that 10 ml of buckwheat honey and 400 mg of immediate release guaifenesin will significantly reduce the frequency and severity of cough compared to placebo over a 4-hour evaluation period.

NCT ID: NCT01058317 Withdrawn - Clinical trials for Recurrent Respiratory Papillomatosis

Propranolol Administration in Pediatric Patients With Recurrent Respiratory Papillomatosis

Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Juvenile onset recurrent respiratory papillomatosis (JORRP) is a rare, difficult to treat, benign tumor of the pediatric airway. Current therapy is mainly surgical, but in a significant portion of patients adjuvant therapy is required to control the disease process. Although multiple adjuvant medical therapies have been tried, success has been limited. We have seen some success in a limited amount of patients using orally administered propranolol. Our goal is to enroll a larger cohort of patients to determine the effectiveness of propranolol as an adjuvant therapy for JORRP.

NCT ID: NCT01057771 Completed - Clinical trials for Acute Respiratory Infection

Meditation and Exercise for Prevention of Acute Respiratory Infection

MEPARI
Start date: June 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The overarching goal of this project is to determine whether mind-body practices such as meditation or exercise can reduce the public health burden of acute respiratory infection. A major secondary goal is to determine whether mindfulness meditation or moderately strenuous exercise can enhance immune processes such as antibody response to influenza vaccination (flu shots). Finally, we want to investigate the influence of stress, optimism, anxiety and positive and negative emotion on immunity and resistance to respiratory infection.

NCT ID: NCT01055990 Active, not recruiting - Influenza Clinical Trials

Basic and Clinical Research on Applying Blood Fix to Treat Critical H1N1 Patients

Start date: October 2009
Phase: Phase 2
Study type: Interventional

The 2009 flu pandemic is a global outbreak of a new strain of influenza A virus subtype H1N1, commonly known as swine flu, that was first identified in April 2009. Large-scale immunization is an essential approach of controlling the pandemic.Vaccines are now becoming available for protection against pandemic influenza A(H1N1) 2009 infection in some countries.In response to the pandemic, novel vaccines against the virus strain A/California/07/2009(H1N1) have been developed and recently were approved for vaccination among specific populations in China. However, the safety and effectiveness of the vaccines is of prime concern to the authorities and the public.This report details the findings of a observational clinical trial of the safety and immunogenicity of a influenza A (H1N1)2009 monovalent vaccine. The virus of Swine Flu H1N1 that outbroke in 2009 is sensitive to neuraminidase inhibitors (Oseltamivir, zanamivir and peramivir) but have drug resistant to adamantanamine derivatives (amantadine and Flumadine), therefore neuraminidase inhibitors are recommended for antiviral therapy against Swine Flu H1N1, effect of which is evidence by the data that such drugs do modify the symptoms and decrease the death rate of H1N1 in America and Mexico. However, clinically, the investigators have encountered that this virus can infect resistant strains of Oseltamivir, which urges for a more effective treatment plan. In view of above situations, seeking for an effective measures against H1N1 flu should be a top priority and will benefit human life and economy globally. This Topic will take the classic strategy of passive immunity to perform basic and clinical researches on applying blood fix to treat critical H1N1 patients and collect blood of healthy persons who are inoculated with specific H1N1 vaccines to cure critical H1N1 patients.

NCT ID: NCT01052961 Completed - Influenza Clinical Trials

A Study on Higher-dose Oseltamivir Treatment's Impact on Viral Clearance and Clinical Recovery in Adults Hospitalized With Influenza

Start date: January 2010
Phase: Phase 4
Study type: Interventional

Adult patients hospitalized with influenza have higher viral loads and more severe illnesses. Thus more aggressive treatment approaches (e.g. higher dose oseltamivir) have been suggested to treat patients suffering from severe influenza infection. The investigators plan to investigate the impact of higher-dose oseltamivir (150 mg b.d.) treatment on viral clearance and clinical recovery in adult patients hospitalized for severe influenza. Such information may lead to optimization of the management strategy used for these patients.

NCT ID: NCT01048073 Completed - Clinical trials for Lower Respiratory Tract Infection

Non-influenza Etiologies of Acute Respiratory Illness in Southeast Asia

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

Acute respiratory infection (ARI) constitutes a leading cause of morbidity, hospitalization and mortality worldwide. The most common etiologic agents of ARI's, especially in children, are viruses. The study objective is to determine the viral and bacterial etiologies of ARIs in patients with lower respiratory tract infection in South East Asia. This is a laboratory based surveillance study, in which the archival specimens from hospitalized patients will be tested for respiratory pathogens other than influenza viruses Standard descriptive statistics will be used to present the findings