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Pneumonia clinical trials

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NCT ID: NCT01217099 Terminated - Clinical trials for Refractory Mycoplasma Pneumoniae Pneumonia

Methylprednisolone Pulse Macrolide Therapy for Refractory Mycoplasma Pneumoniae Pneumonia in Children

MPP
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is planned to investigate whether small doses of methylprednisolone pulse macrolide therapy can relieve symptoms,chest X-rays faster than macrolide alone therapy for refractory mycoplasma pneumoniae pneumonia(MPP) .

NCT ID: NCT01198626 Terminated - Clinical trials for Community-Acquired Bacterial Pneumonia (CABP)

Efficacy and Safety Study of JNJ-32729463 Compared With Moxifloxacin for the Treatment of Subjects Requiring Hospitalization for Community-Acquired Bacterial Pneumonia

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy, safety and tolerability of JNJ-32729463 compared to moxifloxacin for the treatment of subjects requiring hospitalization for Community-Acquired Bacterial Pneumonia (CABP).

NCT ID: NCT01151527 Terminated - Clinical trials for Idiopathic Interstitial Pneumonias

Peripheral Blood Biomarkers in Idiopathic Interstitial Pneumonias

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

We hypothesize that a peripheral blood biomarker or biological signature (gene or protein expression pattern) of idiopathic interstitial pneumonias (IIPs) will simplify and improve the accuracy of diagnosis of IIP and diagnose individuals at an earlier, more treatable, stage of their disease.

NCT ID: NCT01138540 Terminated - Clinical trials for Ventilator Associated Pneumonia

The Gravity-VAP (Ventilator-Associated Pneumonia) Trial

Gravity-VAP
Start date: November 2010
Phase: Phase 3
Study type: Interventional

This study is planned to compare, in patients sedated, intubated and mechanically ventilated, the efficacy and safety of the Lateral Trendelenburg position in comparison to the Semirecumbent Position to prevent incidence of ventilator-associated pneumonia (VAP).

NCT ID: NCT01110421 Terminated - Clinical trials for Pneumonia, Bacterial

A Safety and Tolerability Study of Doripenem Compared With Cefepime in Hospitalized Children With Bacterial Pneumonia

Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of doripenem compared to cefepime in children hospitalized with pneumonia.

NCT ID: NCT01081964 Terminated - Clinical trials for Community Acquired Pneumonia

Safety and Efficacy Study of Oral Zabofloxacin in Community Acquired Pneumonia

Start date: March 2010
Phase: Phase 2
Study type: Interventional

A double-blind, three-arm study, to evaluate the safety and efficacy of two dosing regimens of zabofloxacin (a fluoroquinolone antibiotic) in community acquired pneumonia.

NCT ID: NCT01057758 Terminated - Pneumonia Clinical Trials

STATIN-VAP STATIN-VAP - STATINs and Ventilator-Associated Pneumonia

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The objective is to assess the efficacy and safety of oral simvastatin in patients with a suspicion of ventilator-associated pneumonia (VAP). The hypothesis of this study is that simvastatin therapy will improve mortality in patients a suspicion of VAP.

NCT ID: NCT01032694 Terminated - Clinical trials for Community-Acquired Pneumonia

Non-Interventional Open Label Prospective Observational Comparative Study On Evaluation Of Compliance Of The Empiric Treatment With Azithromycin SR Versus Amoxiclav 1000 Mg In Adult Patients With Mild To Moderate Community Acquired Pneumonia

PROSTO
Start date: April 2010
Phase: N/A
Study type: Observational

To compare compliance between patients with CAP treated with Azithromycin SR 2.0 g single dose orally and those treated with Amoxiclav - 1000 mg twice daily 10 days for the empiric treatment of CAP in outpatient clinic practice.

NCT ID: NCT01014364 Terminated - Pneumonia, Viral Clinical Trials

Low Doses Corticosteroids as Adjuvant Therapy for the Treatment of Severe H1N1 Flu

CORTIFLU
Start date: March 2010
Phase: Phase 3
Study type: Interventional

The H1N1 flu pandemic is one of the major infectious threat of the past half century. it is rapidly progressing worldwide and a substantial number of patients get severe H1N1 related pneumonia that requires mechanical ventilation and admission to the intensive care unit. The acute respiratory distress syndrome is associated with a substantial mortality and morbidity partly as a consequence of uncontrolled lung and systemic inflammation. many physicians are trying to counteract this pro-inflammatory storm by the use of corticosteroids albeit these drugs may cause super infection or metabolic disorders. Thus, there is a need for a randomized double blind, placebo controlled trial to define the benefit to risk ratio of corticosteroids in this patient.

NCT ID: NCT00950027 Terminated - Clinical trials for Ventilator Associated Pneumonia

Study of Povidone Iodine to Reduce Pulmonary Infection in Head Trauma and Cerebral Hemorrhage in Intensive Care Unit

SPIRIT-ICU
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Head trauma and severe cerebral hemorrhage are major risk factors for development of ventilator-associated pneumonia. In a previous open labelled, single center study the investigators showed that repeated oropharyngeal decontamination with povidone-iodine may be an effective strategy to decrease the prevalence of ventilator-associated pneumonia in patients with head trauma. The present study aims to confirm these results in a multicenter, double blind study including patients suffering from head trauma or cerebral hemorrhage.