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Chlorhexidine Gluconate Versus Mupirocin Ointment in the Prevention of Peritoneal Dialysis-Related Infection (COSMO-PD)

Primary Purpose

End Stage Renal Disease, Peritoneal Dialysis

Status
Unknown status
Phase
Phase 4
Locations
Thailand
Study Type
Interventional
Intervention
Chlorhexidine gluconate-soaked cloths
Normal saline
mupirocin ointment
Sponsored by
Chiang Mai University
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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:

  1. History of psychological illness or condition that interferes with the ability to understand or comply with the requirements of the study
  2. Recent (within 1 month) exit-site or tunnel infection, or peritonitis
  3. Known hypersensitivity to, or intolerance of, chlorhexidine gluconate, or mupirocin
  4. Current or recent (within 1 month) treatment with antibiotics administered by any route
  5. 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

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Chlorhexidine gluconate

Normal saline (usual care)

Mupirocin ointment

Arm Description

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

Outcomes

Primary Outcome Measures

Incidence of PD-related infections
Peritonitis or exit-site and tunnel infection

Secondary Outcome Measures

Incidence of infection-related catheter removal
Peritonitis or exit-site and tunnel infection-related catheter removal
Incidence of hospitalization due to PD-related infection
Incidence of PD technical failure (change of modal of dialysis)
change of modal of dialysis
Incidence of death due to PD-related infection
Death due to peritonitis or exit-site and tunnel infection
Rate of Staphylococcus aureus colonization
Incidence of nasal or exit-site S. aureus colonization
Changes in health-related quality of life
Using the Kidney Disease Quality of Life-36 (KDQOL-36), EuroQoL-5 dimension-5 level (EQ-5D-5L)
Number of participants with depression
Using the Beck Depression Inventory II (BDI-II)
Changes in medication adherence
Using (i) directly observed to record the use of investigational medicinal products via return plastic sachets and ointment tubes; (ii) global rating on medication adherence by visual analog scale; and (iii) Medication-taking behavior measure for Thai patients (MTB-Thai questionnaire
Total healthcare costs
Direct medical costs, direct non-medical costs, and indirect costs
Incidence of skin reactions

Full Information

First Posted
September 7, 2015
Last Updated
July 26, 2019
Sponsor
Chiang Mai University
Collaborators
Health Systems Research Institute, Thailand
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1. Study Identification

Unique Protocol Identification Number
NCT02547103
Brief Title
Chlorhexidine Gluconate Versus Mupirocin Ointment in the Prevention of Peritoneal Dialysis-Related Infection
Acronym
COSMO-PD
Official Title
Efficacy and Safety of Local Application of Chlorhexidine Gluconate Versus Mupirocin Ointment in the Prevention of Peritoneal Dialysis-Related Infection: A Double-Blind, Stratified Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2016 (Actual)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
August 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chiang Mai University
Collaborators
Health Systems Research Institute, Thailand

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This pilot study aims to evaluate effectiveness, safety, and cost-utility of chlorhexidine gluconate (CHG)-soaked cloths compares to mupirocin ointment and exit site usual care (normal saline) with aseptic technique in prevention of PD-related infection. It is a multicenter, double-blind, stratified randomized controlled trial. Participants will be randomized to three arms mupirocin, usual care, or CHG-soaked cloths in a ratio of 1:1:1. They will be followed up 24 months or completion of PD. The primary outcome is PD-related infection (PD-related peritonitis of exit-site and tunnel infection). Secondary outcomes are infection-related catheter removal and technique failure, nasal and exit-site Staphylococcus aureus colonization, health-related quality of life, mental health, medication adherence, safety, adverse events related to treatments such as skin irritation, rash, etc. Costs include providers and patients expenses. The utility is assessed using the EuroQol (EQ), five-dimensional (5D), five-level (5L) version. The results of this study are anticipated nephrologists and health care professional involving to PD in decision-making for a plan to prevent PD-related infection. In addition, the results will lead to clinical guideline development a prevention of PD-related infection.
Detailed Description
Peritoneal dialysis (PD) is one of renal replacement therapy used for end-stage renal disease. Since 2011, there has been increasing numbers of patients under "PD First" policy of the Thai government. The most common PD related complication is PD-related infection categorized PD-related peritonitis, and exit site and tunnel infection. Although possible to treat PD-related infection, the incidence of technical failure and death due to peritonitis are still high in Thailand. PD-related infections mainly caused by Staphylococcus aureus. To prevent PD-related infection, cleaning with aseptic solvents using aseptic technique and prevent infection by prescribing prophylactic antibiotics are recommended. The International Society for Peritoneal Dialysis (ISPD) has recommended position statement of the regular use of mupirocin ointment around the catheter exits point and apply in nasal cavity. However, there is rising concern of long term use of mupirocin for mupirocin resistance of S. aureus. CHG is antiseptic use in clinical practice. It can coat at least 12 hours on skin and has anti-bacterial covered in both grams negative and positive. Several meta-analysis studies showed effectiveness of CHG in the prevention of hospitals infection i.e. reduces catheter-related sepsis, postoperative infection, and microbial resistance. According to PD-related infection, CHG has very little evidence of its effectiveness. This pilot study aims to evaluate effectiveness, safety, and cost-utility of CHG-soaked cloths compares to mupirocin ointment and exit site usual care (normal saline and povidone-iodine) with aseptic technique in prevention of PD-related infections. It is a multicenter, double-blind, stratified randomized controlled trial. Participants will be randomized to three arms mupirocin, usual care, or CHG-soaked cloths. They will be followed up 24 months or completetion of PD. The primary outcome is PD-related infection (PD-related peritonitis or exit-site and tunnel infection). Secondary outcomes are infection-related catheter removal and technique failure, nasal and exit-site Staphylococcus aureus colonization, health-related quality of life, mental health, medication adherence, safety, adverse events related to treatments such as skin irritation, rash, etc. For cost-utility analysis, costs include providers and patients expenses. The Utility is assessed using EQ-5D-5L.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease, Peritoneal Dialysis
Keywords
Chlorhexidine gluconate, Mupirocin ointment, Normal saline, Peritonitis, Peritoneal dialysis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
354 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Chlorhexidine gluconate
Arm Type
Experimental
Arm Description
Chlorhexidine gluconate-soaked cloths, clean topical area around catheter exit site with CHG 2% soaked cloths
Arm Title
Normal saline (usual care)
Arm Type
Active Comparator
Arm Description
Normal saline, clean topical area around catheter exit site
Arm Title
Mupirocin ointment
Arm Type
Active Comparator
Arm Description
Mupirocin ointment 2%, clean topical area around catheter exit site with Mupirocin ointment
Intervention Type
Other
Intervention Name(s)
Chlorhexidine gluconate-soaked cloths
Intervention Type
Other
Intervention Name(s)
Normal saline
Intervention Type
Other
Intervention Name(s)
mupirocin ointment
Primary Outcome Measure Information:
Title
Incidence of PD-related infections
Description
Peritonitis or exit-site and tunnel infection
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Incidence of infection-related catheter removal
Description
Peritonitis or exit-site and tunnel infection-related catheter removal
Time Frame
24 months
Title
Incidence of hospitalization due to PD-related infection
Time Frame
24 months
Title
Incidence of PD technical failure (change of modal of dialysis)
Description
change of modal of dialysis
Time Frame
24 months
Title
Incidence of death due to PD-related infection
Description
Death due to peritonitis or exit-site and tunnel infection
Time Frame
24 months
Title
Rate of Staphylococcus aureus colonization
Description
Incidence of nasal or exit-site S. aureus colonization
Time Frame
24 months
Title
Changes in health-related quality of life
Description
Using the Kidney Disease Quality of Life-36 (KDQOL-36), EuroQoL-5 dimension-5 level (EQ-5D-5L)
Time Frame
24 months
Title
Number of participants with depression
Description
Using the Beck Depression Inventory II (BDI-II)
Time Frame
24 months
Title
Changes in medication adherence
Description
Using (i) directly observed to record the use of investigational medicinal products via return plastic sachets and ointment tubes; (ii) global rating on medication adherence by visual analog scale; and (iii) Medication-taking behavior measure for Thai patients (MTB-Thai questionnaire
Time Frame
24 months
Title
Total healthcare costs
Description
Direct medical costs, direct non-medical costs, and indirect costs
Time Frame
24 months
Title
Incidence of skin reactions
Time Frame
24 months
Other Pre-specified Outcome Measures:
Title
Safety profiles
Description
Safety of investigational medicinal products related to potential harm (e.g. participant survival, hospitalization, and emergency visit)
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Surapon Nochaiwong
Phone
+6653991507
Email
surapon.nochaiwong@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Chidchanok Ruengorn
Phone
+6653991507
Email
mei.ruengorn@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chidchanok Ruengorn
Organizational Affiliation
Faculty of Pharmacy CMU
Official's Role
Study Director
Facility Information:
Facility Name
Maharaj Nakorn Chiang Mai Hospital
City
Chiang Mai
ZIP/Postal Code
50200
Country
Thailand
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kajohnsak Noppakun, Nephrologist
Phone
+6653946452
Email
knoppaku@med.cmu.ac.th
First Name & Middle Initial & Last Name & Degree
Chayutthaphong Chaisai, Pharmacist
Phone
+6653941507
Email
c.chayutthaphong@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31856900
Citation
Nochaiwong S, Ruengorn C, Noppakun K, Panyathong S, Dandecha P, Sood MM, Saenjum C, Awiphan R, Sirilun S, Mongkhon P, Chongruksut W, Thavorn K; Thai Renal Outcomes Research (THOR) Investigators. Comparative Effectiveness of Local Application of Chlorhexidine Gluconate, Mupirocin Ointment, and Normal Saline for the Prevention of Peritoneal Dialysis-related Infections (COSMO-PD Trial): a multicenter randomized, double-blind, controlled protocol. Trials. 2019 Dec 19;20(1):754. doi: 10.1186/s13063-019-3953-8.
Results Reference
derived
Links:
URL
http://www.pharmacy.cmu.ac.th
Description
Faculty of Pharmacy, Chiang Mai University

Learn more about this trial

Chlorhexidine Gluconate Versus Mupirocin Ointment in the Prevention of Peritoneal Dialysis-Related Infection

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