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Recruiting Not applicable NCT06343727

A High Protein Egg White Pudding for People With Kidney Failure (HiPE KF)

No applicable phase (e.g. observational)
Conditions: Kidney Failure Frailty Kidney Disease, Chronic

Sponsor: Seven Oaks Hospital Chronic Disease Innovation Centre

trial.available_in: БГ
Overview
The goal of this clinical trial is to compare protein supplements in patients with kidney failure on dialysis. The main questions it aims to answer are: * To determine whether the supplementation of egg white protein pudding in a population of individuals with kidney failure on dialysis is feasible. * To determine whether egg white protein pudding supplementation improves serum albumin similar to other standard nutritional supplements. * To determine the effects of the egg white protein pudding on frailty measures, dietary intakes and analytes in the blood. Participants will receive either the egg white pudding (experimental) or control (Ensure plus) at the end of their dialysis treatments 3-days per week for 12 weeks.
Who can participate
Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the trial * Male or female aged ≥18 years with CKD * On chronic in-center hemodialysis for \> 3 months * Serum albumin \<35 g/L * No expected change in dialysis modality or relocation outside of Winnipeg during the intervention period (12 weeks) Exclusion Criteria: * Allergy to eggs * History of renal transplant * Serum albumin ≥ 35 g/L * Bowel diseases * Cancer * Pregnancy * Receiving chemotherapy treatment * Inability to consume treatment product * Allergy to study treatment ingredients * Planning on starting an exercise program during the duration of the trial * Inability to obtain written informed consent
Interventions
Egg white protein pudding
DIETARY_SUPPLEMENT
: Ensure Plus
DIETARY_SUPPLEMENT
Locations 2
Canada (2)
Seven Oaks General Hospital
Winnipeg , Manitoba
Navdeep Tangri, PhD, MD
Health Science Centre
Winnipeg , Manitoba
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
25.07.2025
Completion date
01.10.2026
Registry ID
NCT06343727
Source
clinicaltrials.gov
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