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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Healthy Volunteers: t
View:

• 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)

Locations
Other Locations
Canada
LHSC Regional Renal Care Program
RECRUITING
London
Contact Information
Primary
Christopher W McIntyre, PhD, MD
christopher.mcintyre@lhsc.on.ca
519-685-8500
Backup
Alireza Akbari, PhD
aakbari@uwo.ca
Time Frame
Start Date: 2018-03-05
Estimated Completion Date: 2026-02-28
Participants
Target number of participants: 400
Treatments
Chronic hemodialysis patients
Patients on standard in-centre 3 times a week hemodialysis
Peritoneal dialysis patients
Patients on peritoneal dialysis
Adult and paediatric patients with CKD stage 1-5
Patients with chronic kidney disease stage 1-5 (not dialysis dependent)
Healthy adult and paediatric controls
Subjects without kidney disease
Heart failure patients with and without renal dysfunction
Heart failure patients (atrial fibrillation etc ...) with and without renal dysfunction
Related Therapeutic Areas
Sponsors
Leads: Chris McIntyre

This content was sourced from clinicaltrials.gov