Peritoneal Dialysis Catheter Exit Site Infection Clinical Trial
Official title:
Chlorhexidine-impregnated Sponge Dressing for Prevention of Catheter Exit Site Infection in Incident Peritoneal Dialysis Patients - a Pilot Study
The purpose of the study is to evaluate the efficacy and safety of chlorhexidine-impregnated disk in preventing catheter exit-site infection in peritoneal dialysis patients
The primary aim of the study is to examine the exit-site infection rate in patients using
chlorhexidine-impregnated dressing.
The participant will be followed up at 2, 6, 12, 24, 36 and 52 weeks of study and during each
visit the catheter exit-site will be examined by one of the investigators for any sign of
infection or allergic reaction, and questionnaires about satisfaction with use of study
material (biopatch) will be asked by a study team member at the 12 week visit of the study.
Each participant will be followed up for one year.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT06022835 -
Chlorhexidine Gluconate-gel Dressing for Exit Site Infection in Peritoneal Dialysis
|
N/A | |
Completed |
NCT02446158 -
Daily Chlorhexidine Care at the Exit Site in Peritoneal Dialysis Patients
|
Phase 4 | |
Active, not recruiting |
NCT05143164 -
Hydrocolloid Dressing for Catheter Exit Site Care in Peritoneal Dialysis Patients
|
N/A | |
Active, not recruiting |
NCT03816111 -
Targeted Education ApproaCH to Improve Peritoneal Dialysis Outcomes Trial
|
N/A |