Clinical Trials Logo

Community-Acquired Pneumonia clinical trials

View clinical trials related to Community-Acquired Pneumonia.

Filter by:

NCT ID: NCT02604628 Completed - Clinical trials for Community-acquired Pneumonia

Increasing Community-acquired Pneumonia Protocol Adherence by Antibiotic Stewardship

CAP-PACT
Start date: November 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of a multifaceted antibiotic stewardship intervention on protocol adherence of moderate-severe community-acquired pneumonia.

NCT ID: NCT02600806 Recruiting - Clinical trials for Community-acquired Pneumonia

Clinical Pathway Based on Procalcitonin Levels for the Management of Community-acquired Pneumonia in Outpatients

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

A clinical protocol was developed for the management of adult outpatients with community-acquired pneumonia (CAP) and Pneumonia Severity Index risk classes I-II. Patients are assigned to oral azithromycin or levofloxacin according to procalcitonin (PCT) levels measured with a rapid point-of-care method. When PCT levels are <0.5 ng/ml, azithromycin, 500 mg/day is given orally for 5 days; if PCT is ≥0.5 ng/ml, levofloxacin, 500 mg/day is given orally for 7 days

NCT ID: NCT02559310 Completed - Clinical trials for Community Acquired Pneumonia

Study to Compare Lefamulin to Moxifloxacin (With or Without Linezolid) for the Treatment of Adults With Pneumonia

LEAP
Start date: September 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the safety and efficacy of lefamulin, a pleuromutilin, for the treatment of adults with moderate to severe community-acquired bacterial pneumonia.

NCT ID: NCT02555852 Completed - Clinical trials for Community-acquired Pneumonia

Proton Pump Inhibitors and Risk of Community-acquired Pneumonia

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

The purpose of the study is to determine whether proton pump inhibitors (PPIs), a medication used to treat gastric conditions, increase the risk of hospitalization for community-acquired pneumonia (HCAP). The investigators will carry out separate population-based cohort studies using administrative health databases in eight jurisdictions in Canada, the US, and the UK. Cohort entry will be defined by the initiation of an oral non-steroidal anti-inflammatory drug, with follow-up until hospitalization for pneumonia or end of follow-up (6 months). The results from the separate sites will be combined using a statistical approach called meta-analysis to provide an overall assessment of the risk of HCAP with PPIs.

NCT ID: NCT02552342 Recruiting - Clinical trials for Community Acquired Pneumonia

Corticosteroid Therapy for Severe Community-Acquired Pneumonia

Start date: May 2015
Phase: Phase 4
Study type: Interventional

The purpose of the present study is to assess the efficacy of methylprednisolone as an adjuvant therapy in patients with severe community-acquired pneumonia (CAP) (PSI 4-5). The hypothesis of the study is that methylprednisolone can decrease the mortality of severe CAP without any significant side effects,with reduction of the time to clinical stability and failure rate of treatment.

NCT ID: NCT02523885 Completed - Clinical trials for Community-acquired Pneumonia

Use of Non Steroidal Antiinflammatory Drugs in Patients With Community Acquired Pneumonia

ALPAJ
Start date: November 2013
Phase: N/A
Study type: Observational

To investigate exposure to nonsteroidal antiinflammatory drugs (NSAIDs) during outpatient management at the early stage of community-acquired pneumonia (CAP) requiring hospital consultation. Non-interventional observational study.

NCT ID: NCT02517489 Completed - Clinical trials for Community Acquired Pneumonia

Community-Acquired Pneumonia : Evaluation of Corticosteroids

CAPE_COD
Start date: October 28, 2015
Phase: Phase 3
Study type: Interventional

Mortality of severe Community-Acquired Pneumonia (CAP) has not declined over time and is between 25 and 30% in sub-groups of patients. Corticosteroids (CTx) could down-regulate pulmonary and systemic inflammation, accelerate clinical resolution and decrease the rate of inflammation-associated systemic complications. Two recent meta-analyses suggest a positive effect on severe CAP day 28 survival when CTx are added to standard therapy. However they are based on only four trials gathering less than 300 patients, of which only one was positive. Recently published guidelines do not recommend CTx as part of CAP treatment. Therefore a well-powered trial appears necessary to test the hypothesis that CTx - and more specifically hydrocortisone - could improve day 28 survival of critically-ill patients with severe CAP, severity being assessed either on a Pulmonary Severity Index ≥ 130 (Fine class V) or by the use of mechanical ventilation or high-FiO2 high-flow oxygen therapy. A phase-III multicenter add-on randomized controlled double-blind superiority trial assessing the efficacy of hydrocortisone vs. placebo on Day 28 all-causes mortality, in addition to antibiotics and supportive care, including the correction of hypoxemia. Randomization will be stratified on: (i) centers; (ii) use of mechanical ventilation at the time of inclusion.

NCT ID: NCT02492425 Not yet recruiting - Clinical trials for Community Acquired Pneumonia

A Registry Study on Hospitalized Patients With Community-acquired Pneumonia in Real-life of China

CAP-China
Start date: January 2016
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the disease burden of hospitalized patients with CAP and HCAP in real life of China

NCT ID: NCT02489578 Unknown status - Clinical trials for Community Acquired Pneumonia

A Retrospective Study on Hospitalized Patients With Community-acquired Pneumonia in China (CAP-China)

RSCAP-China
Start date: July 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the disease burden of hospitalized patients with CAP and healthcare-associated pneumonia (HCAP) in real life of China .

NCT ID: NCT02454114 Completed - Clinical trials for Community Acquired Pneumonia

HOME FIRST Pilot: a Study of Early Supported Discharge in Patients With Lower Respiratory Tract Infections

HOMEFIRST
Start date: October 2013
Phase: N/A
Study type: Interventional

HOME FIRST (Home Followed - up with Infection Respiratory Support Team) is an early supported discharge scheme. It will enable patients with lower respiratory tract infection (LRTI) to be provided with high quality safe, effective, efficient patient centred care, tailored to their needs in their own home; aiming to improve the overall experience of the service user, improve patient outcomes and reduce hospital length of stay whilst simultaneously reducing admission rates, an area of major strategic importance to the NHS.