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Community-Acquired Pneumonia clinical trials

View clinical trials related to Community-Acquired Pneumonia.

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NCT ID: NCT01561885 Completed - Asthma Clinical Trials

Collaborative Healthcare Professionals Approach in Monitoring of Patient Centered Outcomes Through Pathways

CHAMP-Path
Start date: March 2012
Phase: N/A
Study type: Interventional

The aim of this study is to determine if by providing a collaborative, integrated pathway-based healthcare compared to the usual healthcare, whether or not this would be superior in reducing the length of hospital stay across five high frequency /high risk medical diagnoses: Acute Venous Thromboembolism, Acute Kidney Injury, Community Acquired Pneumonia, Adult Left Ventricular Heart Failure, and Asthma.

NCT ID: NCT01537250 Completed - Clinical trials for Community-acquired Pneumonia

Phase II Clinical Study to Assess the Efficacy and Safety of Nemonoxacin Malate in Treating Adult Patients With Community-acquired Pneumonia (CAP)

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

The purpose of this study is to evaluate the safety, tolerability and population pharmacokinetics of oral nemonoxacin in community-acquired pneumonia (CAP) subjects.

NCT ID: NCT01530763 Completed - Infections Clinical Trials

Safety and Efficacy Study of Ceftaroline Versus a Comparator in Pediatric Subjects With Community Acquired Bacterial Pneumonia (CABP)

Start date: September 2012
Phase: Phase 2/Phase 3
Study type: Interventional

This is a study of safety and effectiveness of ceftaroline fosamil in children with Community Acquired Bacterial Pneumonia receiving antibiotic therapy in the hospital.

NCT ID: NCT01420744 Completed - Clinical trials for Community Acquired Pneumonia

Safety and Efficacy Study of BT086 to Evaluate Adjunctive Therapy in sCAP

CIGMA
Start date: August 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the adjunctive therapy to standard antibiotic treatment of BT086 is safe and effective of decreasing the days patients require endotracheal ventilation due to Severe Community-Acquired Pneumonia (sCAP).

NCT ID: NCT01336036 Completed - Clinical trials for Community Acquired Pneumonia

Causes and Outcomes of Community Acquired Pneumonia

CAP
Start date: February 2011
Phase: N/A
Study type: Observational

This is a descriptive clinical research aiming: - To describe the clinical spectrum and clinical characteristics of community acquired pneumonia (CAP) in patients admitted to hospital - To identify the etiology of CAP and the antibiotic sensitivity of the isolated organisms - To identify the risk factors that influence the severity of CAP

NCT ID: NCT01285869 Completed - Clinical trials for Community-acquired Pneumonia

Impact of a Multidimensional Intervention in Elderly Patients With Pneumonia

IMIEPAP
Start date: November 2010
Phase: N/A
Study type: Interventional

The hypothesis of this study is that long-term outcome in elderly patients admitted with the diagnosis of community-acquired pneumonia (CAP) or healthcare-associated pneumonia (HCAP) would improve with a multidimensional intervention including assessment of co-morbidities, nutritional, functional and cognitive status and immunization.

NCT ID: NCT01236677 Recruiting - Clinical trials for Community Acquired Pneumonia

The Establishment and Improvement of Community Acquired Pneumonia Monitoring and Disposal Network in Beijing

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

In the 21st century, threats to human health of new respiratory infectious diseases increased. The project aim is to establish pneumonia pathogens network in Beijing and understand the pathogen spectrum distribution.

NCT ID: NCT01228110 Completed - Clinical trials for Community Acquired Pneumonia

Corticosteroids in Community Acquired Pneumonea

Start date: n/a
Phase: N/A
Study type: Interventional

Low dose hydrocortisone IV in patients with CAP fastens recovery of pneumonia and prevents the development of sepsis related complications with a significant reduction in duration of mechanical ventilation

NCT ID: NCT01200706 Completed - Clinical trials for Community-acquired Pneumonia

Clinical Efficacy of Amoxicillin Given Twice or Three Times a Day Among Children With Non-severe Pneumonia

PNEUMOPACEf
Start date: November 2006
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare the clinical efficacy of amoxicillin given twice or three times a day to children with non-severe community-acquired pneumonia.

NCT ID: NCT01166932 Completed - Clinical trials for Community-Acquired Pneumonia

Comparison Between Amoxycillin/Clavulanic Acid and Oxacillin/Ceftriaxone for Community Acquired-pneumonia

Start date: April 2005
Phase: Phase 4
Study type: Interventional

Objective: To compare the clinical effectiveness and hospital costs, the initial empirical treatment, Oxacillin / Ceftriaxone and Amoxicillin / Clavulanate in children with Community Acquired Pneumonia (CAP) severe. Methods: Clinical prospective randomized study in children aged two months to five years of age with a diagnosis of severe CAP, according to criteria of World Health Organization (WHO), admitted to the Pediatrics Ward of the Hospital of the Medical School of Botucatu- UNESP. We excluded children with comorbid disorders (primary and secondary immunodeficiency) with acute or chronic kidney disease, referred patients receiving antibiotics proposal and history of allergy to antibiotics proposed. We included 104 children who were randomized into two groups to receive: Oxacillin / Ceftriaxone IV (GCO, n = 48) and Amoxicillin / Clavulanate IV (GAA, n = 56). Patients of the GAA, after clinical improvement, has been receiving the same oral antibiotic, and maintaining clinical stability, were discharged from hospital, the GOC received any IV treatment. The outcomes analyzed were time to clinical improvement (fever and tachypnea), duration of oxygen therapy, hospitalization time, need to expand the antimicrobial spectrum progression to pleural effusion / empyema (DP / E) and hospital costs. Treatment failure was determined by the need to expand the antimicrobial spectrum after 48 hours of hospitalization.