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Investigation of the Effects of Medium Cut-off Dialyzers Versus High-Flux Dialyzers on Clinical and Laboratory Parameters of Prevalent Hemodialysis Patients

S

Sanliurfa Mehmet Akif Inan Education and Research Hospital

Status

Completed

Conditions

Anemia of Chronic Kidney Disease
Hemodialysis-Associated Pruritus
Restless Legs Syndrome
Depressive Disorder
Malnutrition-Inflammation-Cachexia Syndrome

Treatments

Device: Dialysis using the FX80 device.
Device: Dialysis using the Theranova-400 device.

Study type

Observational

Funder types

Other

Identifiers

NCT05698420
MCOx_MAIEAH_001

Details and patient eligibility

About

In this study, the investigators aimed to observe the effects of medium cut-off dialysis filters and high-flux dialysis filters on malnutrition inflammation score, uremic itching, restless leg syndrome, anemia, and ESA treatment, which are prominent complications in hemodialysis, and routine follow-up parameters.

Full description

The study is designed as a single-center, prospective, observational research. A total of 50 stable-course chronic hemodialysis patients over 18 years of age and treated for at least 3 months will be included in the study and the study period will be planned for 12 months. 25 of the 50 chronic hemodialysis patients planned to be included in the study will use MCO-membrane and the other 25 will use high-flux membrane. The distribution of patients to the high-flux membrane and MCO membrane groups will be done randomly (sequentially single-pair number method). Then, the standard 12-hour (3x4 hours/week) hemodialysis treatment will continue. At the beginning of the study (0.), at the end of the third (3.) month and at the end of the sixth (6.) month;

Monthly laboratory tests routinely performed on hemodialysis patients (tests routinely performed in hemodialysis patient follow-up) 5 ml blood samples will be taken from the hemodialysis set to determine the levels of medium-large molecule-weight toxins-wastes and inflammatory parameters before and after dialysis, and the sera will be separated and stored at -80oC for use at the end of the study.

Automatic blood pressure measurement will be performed before and after hemodialysis to evaluate arterial stiffness.

The Malnutrition Inflammation Score will be applied to evaluate the nutritional status (the MIS form is given in the appendix) Visual Analog Scale will be used for appetite Visual Analog Scale will be used for uremic pruritus Depression scale screening (Beck's scale)

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic hemodialysis patients
  • Patients continuing the hemodialysis program for at least 3 months
  • Patients over 18 years of age

Exclusion criteria

  • Patients with advanced heart failure, malignancy, terminal illness
  • Patients with active infectious disease
  • Acute hemodialysis patients
  • Patients vascular access dysfunction

Trial design

50 participants in 2 patient groups

The Theranova 400 group, also known as the MCO group.
Description:
Patients undergoing maintenance hemodialysis will receive dialysis treatment using the Theranova 400 device.
Treatment:
Device: Dialysis using the Theranova-400 device.
The FX80 group, also known as the high-flux group.
Description:
Patients undergoing maintenance hemodialysis will receive dialysis treatment using the FX80 device.
Treatment:
Device: Dialysis using the FX80 device.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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