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NCT04824885Completed

Study of a Dialysate Without Acetate on Protein Energy Wasting Syndrome in Chronic Hemodialysis Patient (EASY)

Study of a Dialysate Without Acetate on Protein Energy Wasting Syndrome in Chronic Hemodialysis Patient

Source: ClinicalTrials.gov · Last updated 12 Mar 2025

Brief summary (registry, in English)

This work aims to study the effect of an acetate-free dialysate on protein-energy wasting syndrome in patients with chronic hemodialysis renal failure, in comparison to a conventional dialysate with acetate. The hypothesis is that a dialysate without acetate would improve patients nutritional status

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
23 Mar 2021
Start date
15 Feb 2022
Primary completion date
6 Mar 2025
Lead sponsor
University Hospital, Clermont-Ferrand
NCT number
NCT04824885

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 15 Feb 2022 to the primary completion date, 6 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Acute event in the 3 months preceding inclusion (infection, surgery).
  • With a psychiatric pathology or cognitive impairment rendering him unable to give informed consent

Other

  • Patient with lower limb amputation more proximal than a transmetatarsal amputation (invalidity of the model for estimating body composition by BCM in this situation)
  • Having a neuromuscular pathology responsible for a motor deficit.
  • Whose life expectancy does not exceed 6 months
  • Pregnant women
  • Patient under guardianship, curatorship or legal protection

Who the study is looking for

  • Major patient;
  • Man or woman ;
  • Treated with intermittent hemodialysis for chronic renal failure;
  • Affiliated with a social security scheme;
  • Having given a signed agreement after detailed explanation of the protocol on the basis of the information sheet and likely to comply with it

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Clermont-Ferrand
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.