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A study on the utility of TAZ/PIPC in the treatment of nosocomial pneumonia - Comparison with MEPM

Not Applicable
Conditions
osocomial pneumonia
Registration Number
JPRN-UMIN000003972
Lead Sponsor
Department of Infection Control and Prevention, Aichi Medical University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
160
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Patients with a history of hypersensitivity to the ingredients of this product, such as shock (2) Children (younger than 16 years old) (3) Patients with infectious mononucleosis (4) Patients receiving sodium valproate (5) Pregnant women, lactating women, or patients possibly to be pregnant (6) Patients with hepatic, renal or cardiac diseases, immunodeficiency, other serious underlying diseases or complications, who have difficulty in evaluation of the efficacy of this product. (7) Patients in the group with severe disease (C group), for whom combination with antimicrobial agents is recommended in the guidelines for treatment of nosocomial pneumonia of the Japanese Respiratory Society (8) Other patients judged to be unsuitable as subjects by the physicians in charge

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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