Skip to main content
OpenTrials
Recruiting

NCT Number: NCT03004547

Sodium Deposition in Soft Tissues of Patients with Kidney Disease

Sodium (Na+) hemostasis is abnormal in CKD patients, and this element can be deposited in the skin, muscle, and skeleton - to cope with long term sodium loading. It is known that sodium stored in this non-osmotically active way, is profoundly inflammatory. Furthermore, inflammation has been associated with several uremic symptoms. The investigators will use novel Na+ MRI imaging to examine the Na+ deposition in the skin, muscle, and skeleton of five groups:1) chronic in-center hemodialysis patients, 2) chronic peritoneal dialysis patients, 3) adult and paediatric patients with CKD stage 1-5 and 4) heart failure patients with and without renal dysfunction 5) sex and age-matched healthy adult and paediatric controls. Additionally, they will investigate the association between sodium deposition in these tissues with uremic symptomatology and biochemical markers of metabolism.

Recruiting

Interested in participating?

Request Info

Key information

Age range

6 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

LHSC Regional Renal Care Program

London, Ontario, Canada

Location status: Recruiting

Location contact

Alireza Akbari, PhD

CONTACT

Christopher W McIntyre, MD, PhD

CONTACT

[email protected]

519-685-8500 ext. 58502

Guido Filler, MD

CONTACT

Jean Theberge, PhD

CONTACT

Timothy Scholl, PhD

CONTACT

About this study

Kidneys have a key role in sodium hemostasis through their excretory function. In patients with chronic kidney disease (CKD), kidney function is impaired; thus, suggesting that sodium handling is abnormal in this setting with long-term sodium loading (from oral intake) and lack of adequate urinary excretion. Yet, sodium concentration needs to stay relatively constant to prevent fatal intra-cellular accumulation, which would result in cell injury and death. In hemodialysis patients, at least a part of this extra sodium is non-osmotically active and deposited in the skin, muscle, and skeleton.

Furthermore, it has become increasingly recognized that sodium (once accumulated in tissues) is directly pro-inflammatory, affecting the innate immune system by regulating the activity of macrophages in skin. This linkage between sodium and inflammation indicates a potential link between sodium deposition and uremic symptoms experienced by patients.

There have been no studies to date examining the sodium deposition in the skin, muscle, and skeleton of patients with different kidney function and renal replacement therapy.

This is a pilot study involving a single center recruiting patients from the prevalent maintenance hemodialysis, peritoneal dialysis , CKD stage 1-5, and heart failure populations of London, Ontario, compared to healthy controls. Once recruited, participants will undergo one study visit with the potential of up to two follow-up visits (on a non-dialysis day for hemodialysis patients). Participants will be followed for up to two years after the first study visit. Each session will include symptom questionnaires, the five times sit to stand and 60-second chair stand test (excluding all children), blood pressure and heart rate measurements, blood work (excluding healthy children and adolescents), urine sampling (excluding those on dialysis), an echocardiogram (excluding healthy controls), and an MRI scan of the lower leg detecting sodium content.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age greater than or equal to 6 years
  • For patients on maintenance hemodialysis or peritoneal dialysis: more than 3 months duration of therapy
  • For patients with CKD stage 1-5: CKD stage 1-5 and no indications to start dialysis
  • For heart failure patients: with or without renal dysfunction
  • For healthy controls: lack of kidney disease, heart failure, liver cirrhosis, and peripheral edema

For subsequent visits (must meet 1 of the below indicators):

  • Change in dialysis prescription
  • Change in renal replacement therapy modality
  • Change in medication
  • Parathyroidectomy
  • Intervention added to or removed from dialysis (i.e. such as but not limited exercise, cooling, and ischemic preconditioning)

Exclusion criteria

  • Pregnant, breastfeeding or intending pregnancy
  • Unable to give consent or understand written information
  • Contraindication to MRI study

Treatment and study plan

Measuring sodium content

Other

Sodium MRI measurement of sodium content in the tissues of all participants

Primary outcomes

  1. Na content in the skin, muscle and skeleton of five cohorts

    Time frame: 2 years

Secondary outcomes

  1. Inflammatory Marker: CRP levels

    Time frame: 2 years

  2. Uremic symptom scores among the different groups

    Time frame: 2 years

  3. Liver function markers

    Time frame: 2 years

  4. Liver damage markers (liver enzymes)

    Time frame: 2 years

  5. cardiac markers (troponin)

    Time frame: 2 years

  6. bone markers (ALP, vitamin D levels)

    Time frame: 2 years

  7. Uremic toxin levels

    Time frame: 3-4 years

  8. Endotoxin levels

    Time frame: 5 years

Study contacts

Contact information is provided by the study sponsor or research team.

Alireza Akbari, PhD

CONTACT

[email protected]

Christopher W McIntyre, PhD, MD

CONTACT

[email protected]

519-685-8500 ext. 58502

Sponsors and collaborators

Lead sponsor

Chris McIntyre

Other

Registry information

Official study title

Evaluation of Sodium Deposition in Soft Tissues of Patients with Kidney Disease and Its Association with Patient Symptomatology

Important dates

Study start
2018
Primary completion
2025
Study completion
2026
First posted
Dec 29, 2016
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.