To Assess the Role of Sphingosine-1-phosphate in the Pathobiology of Pneumonia: Generate a New Strategy for Treatment of Severe Community-acquired Pneumonia

Who is this study for? Patients with severe community-acquired pneumonia
What treatments are being studied? Methylprednisolone Sodium Succinate
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

Pneumonia is a major infectious cause of death worldwide and imposes a considerable burden on healthcare resources. Sphingosine-1-phosphate (S1P) is a bioactive sphingolipid and involved in many physiological processes including immune responses and endothelial barrier integrity. In term of endothelial barrier integrity, S1P plays a crucial role in protecting lungs from pulmonary leak and lung injury. Because of the involvement in lung injury, S1P could be the potential biomarker of pneumonia. Recently, our pilot study suggested that patients with CAP have significantly higher plasma S1P levels than healthy individuals. Interestingly, our observational study also showed significantly elevated S1P level in the patients who were treated with methylprednisolone during the hospitalization. Based on the above evidence, we hypothesize that S1P plays an important role in the pathobiology of pneumonia. Moreover, S1P is not only a useful biomarker for diagnosis of CAP, but also can be an indicator for using corticosteroids adjuvant therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Clinical symptoms suggestive community-acquired pneumonia and pneumonia severe index (PSI) \> 90, Age 18 years or older and Written informed consent obtained

Locations
Other Locations
Taiwan
Wan Fang Hospital
RECRUITING
Taipei
Contact Information
Primary
Shih-Chang Hsu, MD
1980bradhsu@gmail.com
0982770936
Time Frame
Start Date: 2019-06-15
Estimated Completion Date: 2025-11
Participants
Target number of participants: 400
Treatments
Experimental: methylprednisolone
20 mg of methylprednisolone IV Q12H for 5 days
Placebo_comparator: Placebo
normal saline IV Q12H for 5 days
Related Therapeutic Areas
Sponsors
Leads: Taipei Medical University WanFang Hospital

This content was sourced from clinicaltrials.gov