Chlorhexidine Gluconate-gel Dressing for Exit Site Infection in Peritoneal Dialysis
NCT06022835 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2023-09-05
Summary
Exit site infection (ESI) is one of the major predisposing factors to peritoneal dialysis (PD) related peritonitis. Chlorhexidine Gluconate (CHG) has been widely used for cutaneous disinfection for half a century. TegadermTM CHG is a water-proof dressing with gel pads that provide 2% CHG to the skin surface and effectively prevents catheter-related infections for intravascular catheters. However, its use has not been accessed in patients with PD catheters. We aim to evaluate the effectiveness of TegadermTM CHG dressing in preventing ESI in PD patients.
Conditions
- Peritoneal Dialysis Catheter Exit Site Infection
- End Stage Renal Disease on Dialysis
- Dialysis; Complications
Interventions
- OTHER
-
Chlorhexidine Gluconate-gel (CHG) Dressing
Participants used Tegaderm™ CHG dressing for 4 months. The dressing was changed every seven days or soiled.
Sponsors & Collaborators
-
National Healthcare Group, Singapore
lead OTHER_GOV
Principal Investigators
-
Allen Yan Lun Liu · Khoo Teck Puat Hospital, Singapore
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 99 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-09-27
- Primary Completion
- 2023-07-31
- Completion
- 2023-07-31
Countries
- Singapore
Study Locations
More Related Trials
-
Effect of the TEGO Connector in Preventing Tunneled Cuffed Hemodialysis Catheters From Dysfunction and/or Bacteremia
NCT01689753 ·Status: COMPLETED ·Phase: NA
-
Chlorhexidine Dressings for Hemodialysis Catheter Exit Site Care: Comparative Study
NCT05855616 ·Status: COMPLETED ·Phase: NA
-
Usefulness of Sterile Adhesive Dressing at the Exit-site of Peritoneal Dialysis Catheter
NCT03677063 ·Status: COMPLETED ·Phase: NA
-
Comparison of Sterile Gauze and Semi-permeable Film Dressing for Hemodialysis Central Venous Catheter
NCT04800575 ·Status: UNKNOWN ·Phase: NA
-
Trial Evaluating the Efficacy of a Chlorhexidine-Impregnated Sponge (BIOPATCH®) to Reduce Catheter-Related Bloodstream Infections in Hemodialysis Patients
NCT00550693 ·Status: COMPLETED ·Phase: PHASE4
-
Point-of-care Test for Diagnosis of Peritonitis in Peritoneal Dialysis Patients
NCT04070196 ·Status: COMPLETED ·Phase: NA
-
Urgent-start Peritoneal Dialysis in ESRD Patients:A Multi-center Study
NCT02946528 ·Status: COMPLETED ·Phase: NA
-
Effect of Icodextrin Solution on Preservation of Residual Renal Function in Patients on Peritoneal Dialysis
NCT01170858 ·Status: COMPLETED ·Phase: NA
-
Check List to Improve Patient Self-care and Product Defect Report in Continuous Ambulatory Peritoneal Dialysis
NCT02755610 ·Status: UNKNOWN ·Phase: NA
-
Chlorhexidine Caps for CLABSI Prevention in Hemodialysis: a Pilot Randomized Controlled Trial
NCT07019610 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Randomised Controlled Trial of Needle Free Access Devices in Preventing Hemodialysis Blood Stream Infection
NCT01082770 ·Status: UNKNOWN ·Phase: PHASE4
-
Comparison of Standard Versus High Dose Urokinase for Dysfunctional Tunneled Dialysis Catheters in Haemodialysis Patients: a Randomized Controlled Trial
NCT06802679 ·Status: COMPLETED ·Phase: PHASE4
-
Long-term Outcome of End-stage Renal Disease Patients Treated With Hig-efficiency Hemodiafiltration
NCT02576873 ·Status: COMPLETED
-
Comparing Super High-flux and High-flux Dialyzer Performance Among Hemodialysis Patient With Sepsis : a Randomized Control Trial
NCT06989892 ·Status: RECRUITING ·Phase: NA
-
Early Feasibility Study to Evaluate the Safety and Efficacy of PAK HD in ESRD Patients
NCT06433193 ·Status: COMPLETED ·Phase: NA
-
Biological Determinants of Peritoneal Dialysis
NCT02694068 ·Status: COMPLETED
-
Incremental PD With Single Icodextrin Exchange
NCT06119373 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Efficacy and Safety Assessments of a Peritoneal Dialysis Solution Containing Glucose, Xylitol, and L-Carnitine in CAPD
NCT04001036 ·Status: TERMINATED ·Phase: PHASE2
-
Observational Study of the Use of Extraneal in Peritoneal Dialysis in Patients
NCT06492031 ·Status: COMPLETED
-
Hemodialysis Infection Prevention Using Polysporin Ointment With Shower Technique in Satellite Centres Pilot Study
NCT02002169 ·Status: UNKNOWN ·Phase: NA
-
Single Versus Combined Antibiotic Therapy for Bacterial Peritonitis in CAPD Patients
NCT01785641 ·Status: COMPLETED ·Phase: NA
-
The Effect of Neutral Peritoneal Dialysis (PD) Solution With Minimal Glucose-Degradation-Product (GDP) on Fluid Status and Body Composition
NCT00966615 ·Status: COMPLETED ·Phase: PHASE4
-
Hemodynamic Efficiency of an Hemodialysis Treatment With High Permeability in Post-resuscitation Shock
NCT00780299 ·Status: COMPLETED ·Phase: PHASE3
-
Occurrence of Emerging Infections After Placement of a Peritoneal Dialysis CatHeter
NCT04730830 ·Status: UNKNOWN ·Phase: NA
-
Ultrafiltration Efficacy of a PD Solution Containing Icodextrin-Xylitol-Carnitine
NCT04086212 ·Status: WITHDRAWN ·Phase: PHASE2