search
Back to results

Dietary Sodium (DS) Intervention to Reduce Volume Overload and Tissue Sodium in Magnetic Resonance Imaging (MRI) for Hemodialysis (HD) Patients (DSMRI)

Primary Purpose

Kidney Failure, Chronic, Dietary Modification

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Observational Control Diet
Controlled Dietary Sodium Restriction
Sponsored by
University of Illinois at Urbana-Champaign
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Failure, Chronic focused on measuring chronic kidney disease, hemodialysis, sodium restriction, MRI

Eligibility Criteria

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

Inclusion Criteria:

  • Willingness to sign informed consent document and age 18 or greater.
  • Willingness to consume intervention meals 3 times per day (with provided snacks) for 30 days.

Exclusion Criteria:

  1. Individuals with pacemakers (exclusion from cardiovascular testing only)
  2. Individuals with major amputations (i.e. whole limb: foot, ankle, leg, arm)
  3. Individuals with ferric metal implants or devices in the body (excluded from MRI testing only)
  4. Claustrophobic individuals (excluded from MRI testing only)
  5. Individuals that do not otherwise meet MRI screening requirements (mentioned below, excluded from MRI testing only)
  6. Individuals on HD therapy <3 days per week or <3 months
  7. Currently following a sodium restricted diet approximately <1,500 mg per day (only excluded from MRI analysis)
  8. Currently diagnosed GI disorder or disease or infection

Sites / Locations

  • University of Illinois at Urbana-ChampaignRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

Participants will follow a Observational Control Diet (CON) diet followed by an Controlled Dietary Sodium Restriction (INT) diet.

Outcomes

Primary Outcome Measures

Interdialytic weight gain
Interdialytic weight from clinic records
Tissue sodium
MRI detected sodium content in the lower leg (mM)

Secondary Outcome Measures

Hydration status
Bio-impedance measured total body water, extracellular fluid, intracellular fluid, and calculated fluid volume overload
Cardiovascular function
Standard blood pressure
Biochemical markers
Vascular endothelial growth factor-C (VEGF-C), C-reactive protein (CRP), interleukin (IL-6), tumour necrosis factor alpha (TNF-a), endothelial nitric oxide (eNOS), serum sodium (Na)
Gut microbiome (stool sample)
DNA sequencing, bacteria phyla and taxa, stool consistency, gastrointestinal symptoms

Full Information

First Posted
June 14, 2017
Last Updated
July 30, 2020
Sponsor
University of Illinois at Urbana-Champaign
Collaborators
Renal Research Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT03189758
Brief Title
Dietary Sodium (DS) Intervention to Reduce Volume Overload and Tissue Sodium in Magnetic Resonance Imaging (MRI) for Hemodialysis (HD) Patients
Acronym
DSMRI
Official Title
Dietary Sodium (DS) Intervention to Reduce Volume Overload and Tissue Sodium in Magnetic Resonance Imaging (MRI) for Hemodialysis (HD) Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 19, 2017 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Illinois at Urbana-Champaign
Collaborators
Renal Research Institute

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
No

5. Study Description

Brief Summary
Sodium-adapted magnetic resonance imaging (23Na-MRI) studies have demonstrated that sodium accumulates in certain tissues, including the skin and skeletal muscle, but may be manipulated by lifestyle factors or therapeutic interventions such as a hemodialysis (HD) session. This tissue sodium accumulation is increased with age and in the presence of certain chronic diseases such as renal failure, and may contribute to the development of high blood pressure. It currently not known what the impact of dietary sodium consumption has on tissue sodium in HD patient's and on the subsequent risk of cardiovascular complications either acutely or chronically. The University of Illinois' Biomedical Imaging Center recently completed safety testing on a 23Na-MRI coil that they modified for measuring skin and muscle sodium levels in the lower leg/calf that will be used for assessing the impact of dietary salt restriction on tissue sodium levels.
Detailed Description
Recent studies illustrate that tissue sodium is regulated by immune cells in interstitial fluids such as the skin and muscle. Localized immune responses in these tissues can promote vascular endothelial growth factor secretion to promote lymphatic release of fluid and electrolytes, which has significant implications for blood pressure control and cardiovascular health. Furthermore, sodium composition of the diet has the potential to promote beneficial gut bacteria in addition to lowering auto-immune response and blood pressure. The purpose of this pilot study is to utilize this 21Na-MRI coil to quantify changes of sodium levels in the skin and skeletal muscle in hemodialysis treatments before and after a low-sodium diet intervention. In this study, all HD patients will undergo a 30-day observation period (CON) followed by a low-sodium diet period (INT) for 30 additional days. Testing will occur at baseline and after each time-point (three time points total). During the CON period, patients will have no changes to their normal dialysis treatment, and will be asked to follow their normal diet. During the INT period, patients will provided a low- sodium diet intervention that includes receiving 3 low sodium meals per day and snacks provided by momsmeals.com. The study outcomes include: clinical outcomes (hospitalizations, treatment efficiency) changes in tissue sodium, cardiovascular measures (blood pressure, cardiac output, and vascular resistance) and fluid/hydration status (total body water, extracellular fluid) using bioelectrical impedance. We will also collect serum to analyze the relationship between changes in tissue sodium and serum minerals (e.g. sodium and potassium), and other factors believed to help regulate tissue sodium levels, including vascular endothelial growth factor (VEGF), and markers of inflammation (CRP, IL-6). Additionally, we plan to collect patient stool samples to analyze how changes in dietary sodium consumption impact the gut microbiome. This study will demonstrate the feasibility of utilizing 23Na-MRI to quantify skin and muscle sodium levels, as well as provide pilot data regarding the relationship between tissue sodium accumulation, inflammation, the gut microbiome, insulin resistance, and cardiovascular health in hemodialysis patients. Results from this study will then be used to design larger trials to investigate related questions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Chronic, Dietary Modification
Keywords
chronic kidney disease, hemodialysis, sodium restriction, MRI

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Observational control followed by dietary intervention
Masking
None (Open Label)
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Participants will follow a Observational Control Diet (CON) diet followed by an Controlled Dietary Sodium Restriction (INT) diet.
Intervention Type
Other
Intervention Name(s)
Observational Control Diet
Other Intervention Name(s)
CON
Intervention Description
Participants will follow their usual or normal diet for 30 days (days 1-30) while under study observation.
Intervention Type
Other
Intervention Name(s)
Controlled Dietary Sodium Restriction
Other Intervention Name(s)
INT
Intervention Description
Participants will be provided with all meals and snacks daily, for 30 days (days 31-60). These meals should meet KDQOI guidelines for energy and protein (30-35 kcal/kg & 1.2 g/kg) as well as low phosphorus, potassium, and sodium. The meals are formulated to less than 600-800 mg sodium each (<2,000g/day) and will be ordered and delivered through momsmeals.com
Primary Outcome Measure Information:
Title
Interdialytic weight gain
Description
Interdialytic weight from clinic records
Time Frame
28 days
Title
Tissue sodium
Description
MRI detected sodium content in the lower leg (mM)
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Hydration status
Description
Bio-impedance measured total body water, extracellular fluid, intracellular fluid, and calculated fluid volume overload
Time Frame
28 days
Title
Cardiovascular function
Description
Standard blood pressure
Time Frame
28 days
Title
Biochemical markers
Description
Vascular endothelial growth factor-C (VEGF-C), C-reactive protein (CRP), interleukin (IL-6), tumour necrosis factor alpha (TNF-a), endothelial nitric oxide (eNOS), serum sodium (Na)
Time Frame
28 days
Title
Gut microbiome (stool sample)
Description
DNA sequencing, bacteria phyla and taxa, stool consistency, gastrointestinal symptoms
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Willingness to sign informed consent document and age 18 or greater. Willingness to consume intervention meals 3 times per day (with provided snacks) for 30 days. Exclusion Criteria: Individuals with pacemakers (exclusion from cardiovascular testing only) Individuals with major amputations (i.e. whole limb: foot, ankle, leg, arm) Individuals with ferric metal implants or devices in the body (excluded from MRI testing only) Claustrophobic individuals (excluded from MRI testing only) Individuals that do not otherwise meet MRI screening requirements (mentioned below, excluded from MRI testing only) Individuals on HD therapy <3 days per week or <3 months Currently following a sodium restricted diet approximately <1,500 mg per day (only excluded from MRI analysis) Currently diagnosed GI disorder or disease or infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Luis M Perez, BS
Phone
7192444805
Email
lmperez2@illinois.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Ken Wilund, PhD
Phone
2172656755
Email
kwilund@illinois.edu
Facility Information:
Facility Name
University of Illinois at Urbana-Champaign
City
Urbana
State/Province
Illinois
ZIP/Postal Code
61801
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ken Wilund, PhD
Phone
217-265-6755
Email
kwilund@illinois.edu
First Name & Middle Initial & Last Name & Degree
Ken Wilund, PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Dietary Sodium (DS) Intervention to Reduce Volume Overload and Tissue Sodium in Magnetic Resonance Imaging (MRI) for Hemodialysis (HD) Patients

We'll reach out to this number within 24 hrs