Chlorhexidine Gluconate Versus Mupirocin Ointment in the Prevention of Peritoneal Dialysis-Related Infection (COSMO-PD)
End Stage Renal Disease, Peritoneal Dialysis
About this trial
This is an interventional prevention trial for End Stage Renal Disease focused on measuring Chlorhexidine gluconate, Mupirocin ointment, Normal saline, Peritonitis, Peritoneal dialysis
Eligibility Criteria
Inclusion Criteria:
1. Patients with end-stage renal disease who were undergoing peritoneal dialysis; either continuous ambulatory peritoneal dialysis (CAPD) or automated peritoneal dialysis (APD)
Exclusion Criteria:
- History of psychological illness or condition that interferes with the ability to understand or comply with the requirements of the study
- Recent (within 1 month) exit-site or tunnel infection, or peritonitis
- Known hypersensitivity to, or intolerance of, chlorhexidine gluconate, or mupirocin
- Current or recent (within 1 month) treatment with antibiotics administered by any route
- Nasal carriage of mupirocin-resistant Staphylococcus aureus or chlorhexidine-resistant S. aureus
Sites / Locations
- Maharaj Nakorn Chiang Mai HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Active Comparator
Chlorhexidine gluconate
Normal saline (usual care)
Mupirocin ointment
Chlorhexidine gluconate-soaked cloths, clean topical area around catheter exit site with CHG 2% soaked cloths
Normal saline, clean topical area around catheter exit site
Mupirocin ointment 2%, clean topical area around catheter exit site with Mupirocin ointment