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Completed NCT05689801

Describe the Effect of the Optimized Hemodialysis Technique (HDx) With Medium Cut-Off Membrane on Recovery Time and Quality of Life

Conditions: Terminal Renal Insufficiency

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 18
Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche

Location: Hôpital Privé Claude Galien Quincy-sous-Sénart

Summary

In this study, the effect of optimizing the dialytic technique using simple questionnaires carried out in clinical routine will be described. More specifically, the conventional dialysis technique will be combined with biofeedback software called HemoControl™. The recovery time and quality of life of patients who will use a polyethersulfone membrane (Revaclear®) and a Medium Cut-Off (MCO) membrane (Theranova®) will be observed. The main objective is to describe the evolution of recovery time after a dialysis session in conventional hemodialysis (HD) on Revaclear® membrane and in so-called optimized hemodialysis (HDx) on MCO membrane, Theranova®.

Eligibility Criteria

Inclusion Criteria: * Patient, male or female (using contraceptives, if of childbearing age), over 18 years of age * Patient on conventional hemodialysis with synthetic membrane for at least 3 months * Patient with a recovery time after the dialysis session ≥ 4 hours * Informed patient who has signed a written consent to participate in the study * Affiliated patient or beneficiary of a social security scheme Exclusion Criteria: * Patient whose seniority of dialysis is less than 3 months * Pregnant woman * Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision * Patient with severe cognitive impairment * Medically unstable or frail patient * Patient who did not sign an informed consent form accepting this research (refusal of consent or absence of signature).

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05689801). StuddyBuddy aggregates publicly available trial information.