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Could Ketoanalogue-supplemented Low Protein Diet Defer Dialysis in Advanced Diabetic Kidney Disease? (K-DDD) (K-DDD)

Primary Purpose

CKD Stage 4

Status
Unknown status
Phase
Not Applicable
Locations
Romania
Study Type
Interventional
Intervention
Protein restriction
Sponsored by
Anemia Working Group Romania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for CKD Stage 4 focused on measuring low protein diet, Diabetic Kidney Disease

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diabetic patients
  • CKD stage 4+ (estimated GFR using the Modification of Diet in Renal Disease 4-variable, MDRD4, formula <30 mL/min per year)
  • stable renal function (historical reduction of eGFR of < 10 ml/min-year)
  • proteinuria > 3g/g creatininuria
  • good nutritional status (SGA A)

Exclusion Criteria:

  • evidence of active kidney disease (except proteinuria)
  • indication for etiological or pathogenic treatment
  • poor control of diabetes (HbA1c >8%)
  • uncontrolled high blood pressure (≥155/85 mmHg)
  • significant co-morbidities (heart failure, active liver disease, malabsorption, active infections, inflammatory diseases requiring corticosteroids)
  • uremic symptoms (pericarditis, digestive disorders
  • or malnutrition (SGA B or C, serum albumin < 3.5 g/dl)

Sites / Locations

  • "Dr Carol Davila" Teaching Hospital of NephrologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Supplemented low protein diet (sLPD)

Mild protein restriction diet (MPD)

Arm Description

Protein restriction to a low level (0.6 g/kg-day, mainly vegetarian) + ketoanalogues of essential amino-acids supplementation (Ketosteril 1 tb/10 kg dry bw)

Mild restriction in dietary protein intake (0.8 g/kg-day)

Outcomes

Primary Outcome Measures

CKD progression
Percentage of patients requiring RRT initiation or a more than 50% reduction in the initial eGFR at anytime during the study

Secondary Outcome Measures

Need for renal replacement therapy (RRT)
Percentage of patients requiring RRT during the study
Patients' Quality of life
Patients' Quality of life, assessed by the SF-36 Questionnaire
Decline in eGFR
Difference between eGFR at any timepoint and the initial eGFR
Correction of nitrogen balance
Serum urea
Correction of metabolic acidosis
Serum bicarbonate
Correction of calcium metabolism abnormalities
Serum calcium
Correction of mineral metabolism abnormalities
Serum phosphates
Serum level of intact Parathyroid Hormone (iPTH)
iPTH
Nutritional status - Subjective Global Assessment (SGA)
SGA
Body Mass Index (BMI)
BMI
Tricipital Skin Fold (TSF)
TSF
Middle arm muscular circumference (MAMC)
MAMC
Serum albumin
Serum albumin
Serum cholesterol
Serum cholesterol
Inflammatory status
Serum C-Reactive Protein (CRP)
Compliance to the protein intake
Achieved protein intake (urinary urea excretion, Mitch-Maroni's formula)
Compliance to the energy intake
Achieved energy intake (3-days food dairy)
Occurence of the adverse events
Occurence of any adverse event

Full Information

First Posted
December 30, 2017
Last Updated
February 21, 2020
Sponsor
Anemia Working Group Romania
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1. Study Identification

Unique Protocol Identification Number
NCT03415074
Brief Title
Could Ketoanalogue-supplemented Low Protein Diet Defer Dialysis in Advanced Diabetic Kidney Disease? (K-DDD)
Acronym
K-DDD
Official Title
Ketoanalogue-supplemented Low Protein Diet and Deferring Dialysis in Patients With Severe Proteinuria and Advanced Diabetic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2019 (Actual)
Primary Completion Date
September 30, 2022 (Anticipated)
Study Completion Date
March 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Anemia Working Group Romania

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 is a prospective single center open label randomized controlled trial aiming to assess the effectiveness and safety of a low protein diet (0.6 g/kg-day, mainly vegetarian) supplemented with ketoanalogues of essential amino-acids (sLPD) as compared to a mild protein restriction (0.8 g/kg-day, MPD) in reducing Chronic Kidney Disease (CKD) progression, with a planned total duration is of 18 months. Adult diabetic patients with CKD stage 4+ [estimated glomerular filtration rate (eGFR) using the Modification of Diet in Renal Disease 4-variable (MDRD4) formula <30 mL/min per year], with stable renal function (historical reduction of eGFR of < 10 ml/min-year) , proteinuria > 3g/g creatininuria and good nutritional status (SGA A) will be enrolled.
Detailed Description
Adult diabetic patients with Chronic Kidney Disease (CKD) stage 4+ (estimated GFR using the Modification of Diet in Renal Disease 4-variable, MDRD4, formula <30 mL/min per year), with stable renal function (historical reduction of eGFR of < 10 ml/min-year), proteinuria > 3g/g creatininuria and good nutritional status (SGA A) will be enrolled. Patients with evidence of active kidney disease (except proteinuria), with indication of etiological or pathogenic treatment, those with poor control of diabetes (HbA1c >8%), those with uncontrolled high blood pressure (≥155/85 mmHg), those with significant co-morbidities (heart failure, active liver disease, malabsorption, active infections, inflammatory diseases requiring corticosteroids), those with uremic symptoms (pericarditis, digestive disorders ) or malnutrition (SGA B or C, serum albumin < 3.5 g/dl) will be excluded. Eligible patients will enter a run-in phase (3 mo), when mild protein restriction (0.8g/kg dry ideal bw) will be initiated and compliance will be evaluated twice monthly. Those who will prove compliant during the run-in phase and still fulfill the selection criteria will be randomized 1:1 (computer-generated numbers) to receive the low protein diet (0.6 g/kg-day, mainly vegetarian) supplemented with ketoanalogues of essential amino-acids (Ketosteril 1 tb/10 kg dry bw) or to continue the mild protein restriction (0.8 g/kg-day). The total recommended energy intake is of 30 kcal/kg of ideal dry body weight per day in all patients. The primary composite endpoint is the need for RRT initiation or a more than 50% reduction in the initial eGFR any time during the assessment phase. The decision to initiate RRT will be made by the Ethical Committee of the Hospital, based on the clinical and laboratory data. The need for RRT initiation, the quality of life [assessed by the Short Form-36 (SF-36) Questionnaire], the decline in GFR and the correction of metabolic complications of CKD [serum levels of urea, calcium, phosphates, serum parathyroid hormone levels, bicarbonate, potassium] will be secondary efficacy parameters. Parameters of nutritional status (SGA, anthropometric and biochemical parameters), compliance to the diet, occurrence of any adverse event and the number of withdrawals will be safety variables. All the parameters will be assessed at baseline, throughout the intervention phase and at end of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
CKD Stage 4
Keywords
low protein diet, Diabetic Kidney Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Eligible patients will enter a run-in phase (3 mo), when mild protein diet (0.8g/kg dry ideal bw) will be initiated and compliance will be evaluated twice monthly. Those who will prove compliant during the run-in phase and still fulfill the selection criteria will be randomized 1:1 (computer-generated numbers) to receive the low protein diet (0.6 g/kg-day, mainly vegetarian) supplemented with ketoanalogues of essential amino-acids (Ketosteril 1 tb/10 kg dry bw) or to continue the mild protein restriction (0.8 g/kg-day).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Supplemented low protein diet (sLPD)
Arm Type
Active Comparator
Arm Description
Protein restriction to a low level (0.6 g/kg-day, mainly vegetarian) + ketoanalogues of essential amino-acids supplementation (Ketosteril 1 tb/10 kg dry bw)
Arm Title
Mild protein restriction diet (MPD)
Arm Type
Active Comparator
Arm Description
Mild restriction in dietary protein intake (0.8 g/kg-day)
Intervention Type
Behavioral
Intervention Name(s)
Protein restriction
Intervention Description
In both arms the dietary protein intake will be reduced. In the sLPD arm, the protein restriction is more severe and ketoanalogues of the essential aminoacids are offered.
Primary Outcome Measure Information:
Title
CKD progression
Description
Percentage of patients requiring RRT initiation or a more than 50% reduction in the initial eGFR at anytime during the study
Time Frame
15 months
Secondary Outcome Measure Information:
Title
Need for renal replacement therapy (RRT)
Description
Percentage of patients requiring RRT during the study
Time Frame
15 months
Title
Patients' Quality of life
Description
Patients' Quality of life, assessed by the SF-36 Questionnaire
Time Frame
at baseline and than every 3 months up to 15 months
Title
Decline in eGFR
Description
Difference between eGFR at any timepoint and the initial eGFR
Time Frame
monthly up to 15 months
Title
Correction of nitrogen balance
Description
Serum urea
Time Frame
monthly up to 15 months
Title
Correction of metabolic acidosis
Description
Serum bicarbonate
Time Frame
monthly up to 15 months
Title
Correction of calcium metabolism abnormalities
Description
Serum calcium
Time Frame
monthly up to 15 months
Title
Correction of mineral metabolism abnormalities
Description
Serum phosphates
Time Frame
monthly up to 15 months
Title
Serum level of intact Parathyroid Hormone (iPTH)
Description
iPTH
Time Frame
monthly up to 15 months
Title
Nutritional status - Subjective Global Assessment (SGA)
Description
SGA
Time Frame
monthly up to 15 months
Title
Body Mass Index (BMI)
Description
BMI
Time Frame
monthly up to 15 months
Title
Tricipital Skin Fold (TSF)
Description
TSF
Time Frame
monthly up to 15 months
Title
Middle arm muscular circumference (MAMC)
Description
MAMC
Time Frame
monthly up to 15 months
Title
Serum albumin
Description
Serum albumin
Time Frame
monthly up to 15 months
Title
Serum cholesterol
Description
Serum cholesterol
Time Frame
monthly up to 15 months
Title
Inflammatory status
Description
Serum C-Reactive Protein (CRP)
Time Frame
monthly up to 15 months
Title
Compliance to the protein intake
Description
Achieved protein intake (urinary urea excretion, Mitch-Maroni's formula)
Time Frame
twice-a-month during the run-in phase, weekly for the first month after randomization, every 4 weeks during the next 6 months, and then every 3 months up to 15 months
Title
Compliance to the energy intake
Description
Achieved energy intake (3-days food dairy)
Time Frame
twice-a-month during the run-in phase, weekly for the first month after randomization, every 4 weeks during the next 6 months, and then every 3 months up to 15 months
Title
Occurence of the adverse events
Description
Occurence of any adverse event
Time Frame
twice-a-month during the run-in phase, weekly for the first month after randomization, every 4 weeks during the next 6 months, and every 3 months up to 15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diabetic patients CKD stage 4+ (estimated GFR using the Modification of Diet in Renal Disease 4-variable, MDRD4, formula <30 mL/min per year) stable renal function (historical reduction of eGFR of < 10 ml/min-year) proteinuria > 3g/g creatininuria good nutritional status (SGA A) Exclusion Criteria: evidence of active kidney disease (except proteinuria) indication for etiological or pathogenic treatment poor control of diabetes (HbA1c >8%) uncontrolled high blood pressure (≥155/85 mmHg) significant co-morbidities (heart failure, active liver disease, malabsorption, active infections, inflammatory diseases requiring corticosteroids) uremic symptoms (pericarditis, digestive disorders or malnutrition (SGA B or C, serum albumin < 3.5 g/dl)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liliana Garneata, Assoc Prof
Phone
+40722619358
Email
lilianagarna@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriel Stefan, MD
Phone
+40724906188
Email
gabriel_stefan@rocketmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriel Mircescu, Prof
Organizational Affiliation
Carol Davila University of Medicine and Pharmacy
Official's Role
Study Chair
Facility Information:
Facility Name
"Dr Carol Davila" Teaching Hospital of Nephrology
City
Bucharest
ZIP/Postal Code
010731
Country
Romania
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liliana Garneata, Assoc Prof
Phone
+40722619358
Email
lilianagarna@yahoo.com
First Name & Middle Initial & Last Name & Degree
Carmen Antonia Mocanu, MD
Phone
+40723673275
Email
carmen_a9@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Unique patient number in the study, biological data; no data to enable patient identification will be provided
IPD Sharing Time Frame
March 2022
Citations:
PubMed Identifier
33389459
Citation
Mihalache A, Garneata L, Mocanu CA, Simionescu TP, Mircescu G. Low-salt low-protein diet and blood pressure control in patients with advanced diabetic kidney disease and heavy proteinuria. Int Urol Nephrol. 2021 Jun;53(6):1197-1207. doi: 10.1007/s11255-020-02717-2. Epub 2021 Jan 2.
Results Reference
derived

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Could Ketoanalogue-supplemented Low Protein Diet Defer Dialysis in Advanced Diabetic Kidney Disease? (K-DDD)

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