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Fecal Microbiota Transplantation as a Therapeutic Strategy in the Progression of Chronic Kidney Disease

Primary Purpose

Chronic Kidney Disease Due to Hypertension, Chronic Kidney Disease Due to Type 2 Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Faecal microbiota transplant
Placebo
Sponsored by
Hospital Universitario Dr. Jose E. Gonzalez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Disease Due to Hypertension focused on measuring chronic kidney disease, fecal microbiota

Eligibility Criteria

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

Inclusion Criteria:

  • Be diagnosed with CKD and creatinine clearance less than 60 ml / minute secondary to hypertension and / or diabetes.
  • Age over 18 years

Exclusion Criteria:

  • Malignant neoplasms whose last treatment was less than 5 years
  • Having received antibiotics for any reason during the month prior to enrollment
  • Have received probiotics in the last 3 months
  • Have been diagnosed with Clostridium difficile infection in the last year
  • Have been previously submitted to TMF
  • Having presented ERC exacerbations during the 3 months prior or present at the time of enrollment

Sites / Locations

  • Hospital Universitario José E. Gonzalez

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Faecal microbiota transplant

Placebo

Arm Description

This group will receive frozen capsules to be ingested orally constituted of TMF with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.

This group will receive frozen capsules to be ingested orally placebo with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.

Outcomes

Primary Outcome Measures

Creatinine Clearance
Arrest CKD progression

Secondary Outcome Measures

24-hour Urine Protein
Arrest CKD progression
Serum Creatinine
Arrest CKD progression
Hemoglobin
Arrest CKD progression
Hematocrit
Arrest CKD progression
Leukocytes
Arrest CKD progression
Neutrophils
Arrest CKD progression
Platelets
Arrest CKD progression
Glucose
Arrest CKD progression
Urea Nitrogen
Arrest CKD progression
Uric Acid
Arrest CKD progression
Albumin
Arrest CKD progression
Reactive Protein C
Arrest CKD progression
Chlorine
Arrest CKD progression
Sodium
Arrest CKD progression
Potassium
Arrest CKD progression
Phosphorous
Arrest CKD progression
pH Venous Gasometry
Arrest CKD progression
CO2 pressure venous
Arrest CKD progression
Venous Bicarbonate
Arrest CKD progression
Base Excess
Arrest CKD progression
Lactate
Arrest CKD progression

Full Information

First Posted
April 22, 2020
Last Updated
April 26, 2020
Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
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1. Study Identification

Unique Protocol Identification Number
NCT04361097
Brief Title
Fecal Microbiota Transplantation as a Therapeutic Strategy in the Progression of Chronic Kidney Disease
Official Title
Fecal Microbiota Transplantation as a Therapeutic Strategy in the Progression of Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
August 7, 2018 (Actual)
Primary Completion Date
November 7, 2019 (Actual)
Study Completion Date
April 21, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Dr. Jose E. Gonzalez

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
What the investigators want to achieve with the protocol is to identify the impact of intestinal microbiota transplantation on the progression of chronic kidney disease. Hypothesis: Modification of intestinal microbioma of CKD patients by TMF decrease the progression of CKD Methodological design: Experimental, prospective, double-blind. Inclusion criteria: Being diagnosed with CKD and creatinine clearance less than 60 mL/minute secondary hypertension and/or diabetes and older than 18 years
Detailed Description
What the investigators want to achieve with the protocol is to identify that impact has transplantation intestinal microbiota on the progression of chronic kidney disease A.-Hypothesis: Modification of intestinal microbioma of CKD patients by TMF decrease the progression of CKD. B.-Specific objectives: Evaluate whether decreases TMF markers of inflammation in patients with CKD after being treated with TMF, evaluate the behavior in CKD progression markers in patients undergoing TMF, evaluate the change in bowel microbioma CKD patients before and after undergoing TMF. C.-Methodological design: Experimental, prospective, double-blind. D.-Type of study: Controlled clinical trial E.- Population in study: -Inclusion criteria: Being diagnosed with CKD and creatinine clearance less than 60 mL/minute secondary hypertension and/or diabetes, older than 18 years. - Exclusion Criteria: Malignancies whose last treatment has been less than 5 years, he is receiving antibiotics for any reason during the month prior to enrollment, having received probiotics in the last 3 months, it has been diagnosed with Clostridium difficile infection in the last year, it has been previously subjected to TMF , exacerbations of submitting ERC during the 3 months prior or present at the time of enrollment. -Criteria for elimination: Failure to comply in the structured patient monitoring, nondelivery of stool samples at set times, the patient decides to no longer participate in the study. F.- Desing Description: After being selected and randomized patients who meet the criteria for inclusion and exclusion, they are assigned to a group to start treatment TMF (capsules intestinal microbiota frozen) or a group receive placebo capsules which shall consist of an excipient harmless to the body (capsules frozen saline), both will be developed in the service Infectología. Both groups receive frozen for ingestion orally capsules (comprised of TMF or placebo according to the randomization) with a frequency of 15 capsules each 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule must be ingested over a period no longer than 1 hour. measurements characteristic factors of the progression of kidney disease day 0,10, 30, 60, 90, 120 and 180 be made consisting of: Proteins in urine 24 hours Creatinine clearance 24 hours CBC serum creatinine Urea Nitrogen Urea Glucose Uric acid IS venous gases Blood samples were taken by puncture of peripheral vein by laboratory personnel to assess renal function, urine samples will be collected by the patient at home and transported to the laboratory, none of these samples will be used for genetic analysis , only samples of faeces they underwent genomic analysis, collection of stool samples will days 0, 5, 10 30, 90 and 180 (on 10, 30, 90 and 180 with a range of +/- 2 days). adverse effects questionnaires on days 1, 5, 30 and 60 is performed and quality of life assessment on days 0, 10, 30, 90 and 180. Monitoring will face on a weekly basis to register if they have submitted infections, adverse effects and whether changes have received treatment. Visits will be made in the epidemiology and the Regional Center for Kidney Diseases University Hospital

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease Due to Hypertension, Chronic Kidney Disease Due to Type 2 Diabetes Mellitus
Keywords
chronic kidney disease, fecal microbiota

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, double blind, experimental
Masking
ParticipantCare ProviderInvestigator
Masking Description
Third party makes the aleatorization
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Faecal microbiota transplant
Arm Type
Experimental
Arm Description
This group will receive frozen capsules to be ingested orally constituted of TMF with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This group will receive frozen capsules to be ingested orally placebo with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.
Intervention Type
Biological
Intervention Name(s)
Faecal microbiota transplant
Intervention Description
Both groups will receive frozen capsules to be ingested orally (constituted of TMF or placebo according to the randomization) with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
Both groups will receive frozen capsules to be ingested orally (constituted of TMF or placebo according to the randomization) with a frequency of 15 capsules every 12hrs for 4 doses on days 1, 10 and 30 of the study. Each capsule should be ingested in a period no longer than 1 hour.
Primary Outcome Measure Information:
Title
Creatinine Clearance
Description
Arrest CKD progression
Time Frame
6 months
Secondary Outcome Measure Information:
Title
24-hour Urine Protein
Description
Arrest CKD progression
Time Frame
6 months
Title
Serum Creatinine
Description
Arrest CKD progression
Time Frame
6 months
Title
Hemoglobin
Description
Arrest CKD progression
Time Frame
6 months
Title
Hematocrit
Description
Arrest CKD progression
Time Frame
6 months
Title
Leukocytes
Description
Arrest CKD progression
Time Frame
6 months
Title
Neutrophils
Description
Arrest CKD progression
Time Frame
6 months
Title
Platelets
Description
Arrest CKD progression
Time Frame
6 months
Title
Glucose
Description
Arrest CKD progression
Time Frame
6 months
Title
Urea Nitrogen
Description
Arrest CKD progression
Time Frame
6 months
Title
Uric Acid
Description
Arrest CKD progression
Time Frame
6 months
Title
Albumin
Description
Arrest CKD progression
Time Frame
6 months
Title
Reactive Protein C
Description
Arrest CKD progression
Time Frame
6 months
Title
Chlorine
Description
Arrest CKD progression
Time Frame
6 months
Title
Sodium
Description
Arrest CKD progression
Time Frame
6 months
Title
Potassium
Description
Arrest CKD progression
Time Frame
6 months
Title
Phosphorous
Description
Arrest CKD progression
Time Frame
6 months
Title
pH Venous Gasometry
Description
Arrest CKD progression
Time Frame
6 months
Title
CO2 pressure venous
Description
Arrest CKD progression
Time Frame
6 months
Title
Venous Bicarbonate
Description
Arrest CKD progression
Time Frame
6 months
Title
Base Excess
Description
Arrest CKD progression
Time Frame
6 months
Title
Lactate
Description
Arrest CKD progression
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Be diagnosed with CKD and creatinine clearance less than 60 ml / minute secondary to hypertension and / or diabetes. Age over 18 years Exclusion Criteria: Malignant neoplasms whose last treatment was less than 5 years Having received antibiotics for any reason during the month prior to enrollment Have received probiotics in the last 3 months Have been diagnosed with Clostridium difficile infection in the last year Have been previously submitted to TMF Having presented ERC exacerbations during the 3 months prior or present at the time of enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adrian Camacho-Ortiz, PhD
Organizational Affiliation
Hospital Universitario "Dr. Jose Eleuterio Gonzalez, UANL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario José E. Gonzalez
City
Monterrey
State/Province
Nuevo Leon
ZIP/Postal Code
64460
Country
Mexico

12. IPD Sharing Statement

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Fecal Microbiota Transplantation as a Therapeutic Strategy in the Progression of Chronic Kidney Disease

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