search
Back to results

Beneficial Effect of Probiotics on Chronic Kidney Disease

Primary Purpose

Chronic Kidney Disease

Status
Completed
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
Probiotics
Cornstarch
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Kidney Disease

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. receiving peritoneal dialysis for more than 3 months, at least 18 years of age, and GFR < 15 ml/min.
  2. receiving hemodialysis dialysis for more than 3 months, at least 18 years of age, and GFR < 15 ml/min.
  3. Stage 3 and 4 CKD patients

Exclusion Criteria:

  • active infectious conditions within the last 30 days,
  • pregnancy for female,
  • autoimmune disease e.g. SLE.,
  • cardiovascular events before.

Sites / Locations

  • China Medical University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Probiotics

Arm Description

cornstarch

probiotics

Outcomes

Primary Outcome Measures

the Occurrence of Cardiovascular Event and Peritonitis Events

Secondary Outcome Measures

Change of Gastrointestinal Symptoms at 6 Months
The change in gastrointestinal symptom rating scale (min and maximum scores 0-45) after treatment. The total score is reported. The higher scale represents a worse outcome.

Full Information

First Posted
July 8, 2011
Last Updated
October 9, 2015
Sponsor
China Medical University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01391468
Brief Title
Beneficial Effect of Probiotics on Chronic Kidney Disease
Official Title
Beneficial Effect of Probiotics on Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
China Medical University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized double blinded placebo control studies are performed in Chronic Kidney Disease (CKD) patients. After informed consent, intervention group receives probiotics containing 109 CFU B. bifidum, B.catenulatum, B. longum, and L.plantarm), while placebo group receives corn starch. In the first year the investigators examine the 60 peritoneal dialysis (PD) patients, in the second year the investigators do the 60 hemodialysis (HD) patients, and in the third year the investigators do the 60 stage 3 and 4 CKD patients. Primary endpoint is cardiovascular event, gastrointestinal symptoms, peritonitis in PD patients, and progression of stage 3 and 4 CKD. Values are compared between the groups by unpaired t test. X2 testis used to compare proportions between the groups. Relative risk and the number needed to treat, both with 95% CI, are used to describe the treatment effect of probiotics. A p value less than 0β€’05 is regarded as statistically significant.
Detailed Description
Chronic kidney disease (CKD) is a global health issue that has a substantial impact on affected individuals. The prognosis of dialysis patients is poor with 30 to 50 percent 5 year survival in nondiabetic patients and 25 percent in diabetics. Cardiovascular disease accounts for approximately half of death of dialysis patients Chronic inflammation, which is widely seen in long-term dialysis patients, is associated with malnutrition, atherosclerosis and an increased mortality risk. Inflammatory markers such as C-reactive protein (CRP),IL-6, Il-18 and TNF-Ξ±, are elevated in dialysis and can predict cardiovascular event and all-cause mortality. Probiotics are microorganisms that have beneficial properties for the host. Three described benefits include suppression of growth or epithelial binding/invasion by pathogenic bacteria, improvement of intestinal barrier function and modulation the immune systems. Several probiotics preparations induce protective cytokines, including IL-10, and suppress proinflammatory cytokines, such as TNF-Ξ± and IL-6. Intestinal microflora is deranged in hemodialysis (HD) patients as an increase in aerobic bacteria such as E. coli and a decrease in anaerobic bacteria such as Bifidobacterium. One study reported that oral administration of ifidobacterium longum in a gastroresistant seamless capsule decreases the the pre-HD serum levels of homocysteine and indoxyl sulfate. Another small-scale study from Japan showed that synbiotics containing lactobacilli and can reduce serum level of p-Cresol in HD patients. High-serum p-cresyl sulfate and indoxyl sulfate levels were associated with renal progression. Serum concentrations of p-cresol are independently associated with overall mortality and cardiovascular disease in HD patients. The aim of the study is 1. to evaluate the difference of intestinal microflora between CKD patients and healthy controls; 2. to evaluate whether the investigators can reduce cardiovascular events in CKD patients, and peritonitis in peritoneal dialysis (PD) patients, retard the progression of stage 3 and 4 CKD patients, and decrease circulating inflammatory markers(CRP, IL-6,IL-18, TNF-Ξ±), indoxyl sulfate, p-cresol and homocysteine after probiotics treatment. Randomized double blinded placebo control studies are performed in CKD patients. After informed consent, intervention group receives probiotics containing 109 CFU B. bifidum, B.catenulatum, B. longum, and L.plantarm), while placebo group receives corn starch. In the first year the investigators examine the 60 PD patients, in the second year the investigators do the 60 HD patients,and in the third year the investigators do the 60 stage 3 and 4 CKD patients. Primary endpoint is cardiovascular event, gastrointestinal symptoms, peritonitis in PD patients, and progression of stage 3 and 4 CKD. Values are compared between the groups by unpaired t test. X2 testis used to compare proportions between the groups. Relative risk and the number needed to treat, both with 95% CI, are used to describe the treatment effect of probiotics. A p value less than 0Β·05 is regarded as statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
cornstarch
Arm Title
Probiotics
Arm Type
Experimental
Arm Description
probiotics
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotics
Intervention Description
intervention group receives probiotics containing 10E9 CFU B. bifidum, B. catenulatum, B. longgim, and L. plantarm in 6 months observations
Intervention Type
Dietary Supplement
Intervention Name(s)
Cornstarch
Intervention Description
placebo will be given in 6 months
Primary Outcome Measure Information:
Title
the Occurrence of Cardiovascular Event and Peritonitis Events
Time Frame
6 month follow-up
Secondary Outcome Measure Information:
Title
Change of Gastrointestinal Symptoms at 6 Months
Description
The change in gastrointestinal symptom rating scale (min and maximum scores 0-45) after treatment. The total score is reported. The higher scale represents a worse outcome.
Time Frame
6 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: receiving peritoneal dialysis for more than 3 months, at least 18 years of age, and GFR < 15 ml/min. receiving hemodialysis dialysis for more than 3 months, at least 18 years of age, and GFR < 15 ml/min. Stage 3 and 4 CKD patients Exclusion Criteria: active infectious conditions within the last 30 days, pregnancy for female, autoimmune disease e.g. SLE., cardiovascular events before.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
I-Kuan Wang, M.D.
Organizational Affiliation
China Medical University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
ZIP/Postal Code
413
Country
Taiwan

12. IPD Sharing Statement

Learn more about this trial

Beneficial Effect of Probiotics on Chronic Kidney Disease

We'll reach out to this number within 24 hrs