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Investigation of methods for preventing biofilm formation in peritoneal dialysis-related peritonitis

Not Applicable
Conditions
End stage renal disease, Peritoneal dialysis-related peritonitis
Registration Number
JPRN-UMIN000038500
Lead Sponsor
Kawashima hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with a history of allergies to macrolide Patients complicated with exit infections and tunnel infections Patients with less than two weeks of treatment periods Patients suspected of biofilm formation due to peritonitis more than four weeks after previous peritonitis, the pathogenic microorganism is the same as previous one, or bacteria could not be detected. Patients without agreement on enrolment of this study Inappropriate patients judged by doctor

Study & Design

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