Anti-Oxidant Effect on Peritoneal Membrane in Peritoneal Dialysis (PD) Patients
Primary Purpose
End-Stage Kidney Disease, Peritoneal Dialysis
Status
Unknown status
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
N-acetylcysteine
Sponsored by
About this trial
This is an interventional treatment trial for End-Stage Kidney Disease focused on measuring Antioxidant, Epithelial to Mesenchymal Transition, peritoneal fibrosis, Peritoneal Dialysis, Continuous Ambulatory
Eligibility Criteria
Inclusion Criteria:
- Maintenance peritoneal dialysis at least 3 months
- Patients who are able and willing to understand, sign and date an informed consent document, and authorize access to protected health information
Exclusion Criteria:
- Episode of peritonitis at least 3 months
- Episodes of admission due to other disease at lease 3 months
- Liver disease
- Allergic history with N-acetylcysteine
Sites / Locations
- Ewha Womans University Mokdong HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
N-acetylcysteine
Arm Description
Age and sex matched peritoneal dialysis patients
N-acetylcysteine in stable peritoneal dialysis patients
Outcomes
Primary Outcome Measures
Peritoneal membrane function
Changes in peritoneal membrane function (Δ D/Pcreatinine, ΔD/Purea) with peritoneal equilibrium test
Secondary Outcome Measures
Oxydative stress status
Measurement of oxydative stress status with plasma and RBC (GSH/GSSG, 8-OHdG)
Mesothelial cell transformation (Epithelial to Mesenchymal Transition)
Morphology was analysed with peritoneal dialysate isolated mesothelial cell
Residual renal function
Changes in residual renal function (ΔKt/Vurea, ΔeGFR)
Peritoneal membrane function
Changes in peritoneal membrane function (Δ D/Pcreatinine, ΔD/Purea) with peritoneal equilibrium test
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01111422
Brief Title
Anti-Oxidant Effect on Peritoneal Membrane in Peritoneal Dialysis (PD) Patients
Official Title
A Randomized Prospective Trial of N-acetyl Cystein in Patients With Peritoneal Dialysis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2010
Overall Recruitment Status
Unknown status
Study Start Date
March 2010 (undefined)
Primary Completion Date
December 2010 (Anticipated)
Study Completion Date
December 2011 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Ewha Womans University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Peritoneal fibrosis is one of the major causes of technical failure in patients on peritoneal dialysis (PD) for long period of time. Although the exact mechanisms of peritoneal damage during PD still remain unclear, generation of reactive oxygen species may be responsible for progressive membrane dysfunction. N-acetylcysteine (NAC)is a powerful antioxidant shown to protect peritoneal fibrosis in peritoneal dialysis animal model. In this study the researchers investigated the hypothesis that NAC protect peritoneal membrane damage.
Detailed Description
N-Acetylcysteine (NAC) is known to be relatively safe and beneficial in peritoneal dialysis patient at a dose of 1200 mg per day. Patients will be randomly assigned to NAC and control group and prescribed according to the protocol. At 2 and 6 month, Peritoneal equilibrium test (PET) will be performed with blood sampling.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-Stage Kidney Disease, Peritoneal Dialysis
Keywords
Antioxidant, Epithelial to Mesenchymal Transition, peritoneal fibrosis, Peritoneal Dialysis, Continuous Ambulatory
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Description
Age and sex matched peritoneal dialysis patients
Arm Title
N-acetylcysteine
Arm Type
Experimental
Arm Description
N-acetylcysteine in stable peritoneal dialysis patients
Intervention Type
Drug
Intervention Name(s)
N-acetylcysteine
Other Intervention Name(s)
Muteran capsuleⓇ HAN WHA PHARM.
Intervention Description
N-acetylcysteine (200 mg/capsule) 1200 mg/day (600 mg bid) for 6 months
Primary Outcome Measure Information:
Title
Peritoneal membrane function
Description
Changes in peritoneal membrane function (Δ D/Pcreatinine, ΔD/Purea) with peritoneal equilibrium test
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Oxydative stress status
Description
Measurement of oxydative stress status with plasma and RBC (GSH/GSSG, 8-OHdG)
Time Frame
6 months
Title
Mesothelial cell transformation (Epithelial to Mesenchymal Transition)
Description
Morphology was analysed with peritoneal dialysate isolated mesothelial cell
Time Frame
6 month
Title
Residual renal function
Description
Changes in residual renal function (ΔKt/Vurea, ΔeGFR)
Time Frame
6 month
Title
Peritoneal membrane function
Description
Changes in peritoneal membrane function (Δ D/Pcreatinine, ΔD/Purea) with peritoneal equilibrium test
Time Frame
2 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Maintenance peritoneal dialysis at least 3 months
Patients who are able and willing to understand, sign and date an informed consent document, and authorize access to protected health information
Exclusion Criteria:
Episode of peritonitis at least 3 months
Episodes of admission due to other disease at lease 3 months
Liver disease
Allergic history with N-acetylcysteine
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mina Yu, MD
Phone
+82-2-2650-2562
Email
yuelizabeth@hanmail.net
First Name & Middle Initial & Last Name or Official Title & Degree
Hyun-Jung Kim, NR
Phone
+82-2-2650-5497
Email
40739@eumc.co.kr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Duk-Hee Kang, MD. PhD.
Organizational Affiliation
Ewha Womans University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ewha Womans University Mokdong Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mina Yu, MD
Phone
+82-2-2650-2562
Email
yuelizabeth@hanmail.net
First Name & Middle Initial & Last Name & Degree
Hyun Jung Kim, Nurse
Phone
+82-2-2650-5497
First Name & Middle Initial & Last Name & Degree
Duk-Hee Kang, Professor
12. IPD Sharing Statement
Learn more about this trial
Anti-Oxidant Effect on Peritoneal Membrane in Peritoneal Dialysis (PD) Patients
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