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A clinical trial to study the effects of two skin antibiotic preparations, Mupirocin and Medihoney applied at the catheter exit site of peritoneal dialysis patients

Phase 2
Conditions
Health Condition 1: null- Prevention of Infection at Tenckhoff Exit Site in Peritoneal Dialysis Patients
Registration Number
CTRI/2011/08/001971
Lead Sponsor
Royal Brisbane Hospital Queensland Australia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
440
Inclusion Criteria

?Chronic Kidney Disease stage 5 patients aged 18 years or older on PD

?Incident and prevalent PD patients willing to provide informed consent

Exclusion Criteria

?History of psychological illness or condition that interferes with ability to understand or comply with the requirements of the study;

?Recent (within 1 month) ESI, peritonitis, or tunnel infection;

?Known hypersensitivity to, or intolerance of, honey or mupirocin;

?Current or recent (within 4 weeks) treatment with an antibiotic administered by any route

Study & Design

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