Skip to main content
Clinical Trials/JPRN-UMIN000008010
JPRN-UMIN000008010
Completed
未知

Clinical study to evaluate anti-inflammatory effects of intravenous azithromycin add-on therapy for the treatment of bacterial pneumonia. - Clinical study to evaluate anti-inflammatory effects of intravenous azithromycin add-on therapy (YCRG0008)

Yokohama City University Medical Center0 sites80 target enrollmentMay 23, 2012
ConditionsPneumonia

Overview

Phase
未知
Intervention
Not specified
Conditions
Pneumonia
Sponsor
Yokohama City University Medical Center
Enrollment
80
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 23, 2012
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Patients with hypersensitivity to azithromycin, macrolide or ketolide antibiotic agents (2\) Patients with hypersensitivity to levofloxacin or ofloxacin (3\) Patients with liver dysfunction (AST, ALT, and total bilirubin \> 3 times upper limit of normal range) (4\) Patients with severe renal dysfunction (creatinine clearance \<30 mL/min) (5\) Patients with prior or current evidence of severe heart diseases (NYHA grade IV), congenital or sporadic prolongation of the QT interval, or receiving medications known to cause prolongation of the QT interval (6\) Patients with severe underlying diseases or complications that have the difficulties of the evaluations of drug efficacy (7\) Patients who require other systemic antibiotic treatments (8\)Patients by whom other antimicrobial drugs (internal use or injection) were prescribed for the patient exceeding 48 hours to this infection before investigational new drug trial drug medication (9\)Patients with gastrointestinal disorders disrupting drug absorption (10\)Pregnant women or females with childbearing potential (11\) Any other condition which, in the opinion of the investigator, would make the subject unsuitable for enrollment

Outcomes

Primary Outcomes

Not specified

Similar Trials