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Clinical Trials/NCT07254897
NCT07254897Not yet recruitingNot Applicable

Long-term Muscle Synthetic Effects of Intradialytic Parenteral Nutrition in Chronic Hemodialysis Patients

Erasmus Medical Center1 site in 1 country16 target enrollmentStarted: January 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
16
Locations
1
Primary Endpoint
Myofibrillar fractional synthetic rate

Study Overview

Brief Summary

This study examines the effects of intradialytic parenteral nutrition (IDPN) on muscle growth and blood pressure in patients undergoing chronic hemodialysis.

Detailed Description

Rationale: Malnutrition and a negative protein balance are highly prevalent in hemodialysis (HD) patients. In these patients, nutritional status and body composition are closely linked to morbidity, mortality, and quality of life. Muscle wasting in HD patients is the result of poor intake, anabolic resistance and the intradialytic loss of amino acids, leading to a negative protein balance. Intradialytic parenteral nutrition (IDPN) has been shown to reverse this anabolic state in the short term (a single dialysis session) in studies using primed constant infusion of isotope-labeled amino acids. However, such studies were carried out in fasted state, which may significantly overestimate the effect. Moreover, they provide no insight in muscle synthesis over longer periods of time, including the interdialytic interval and across multiple dialysis sessions. The use of deuterated water (2H2O) enables longer-term assessment of muscle protein synthesis in an outpatient setting. The administration of IDPN, due to its volume, may have intradialytic hemodynamic effects, which have not been characterized in previous studies.

Objective: To study the effect of IDPN on muscle protein synthesis in chronic hemodialysis patients and to characterize the hemodynamic effects of IDPN.

Study design: Investigator-initiated intervention study with crossover design.

Study population: Chronic hemodialysis patients aged over 18 years (dialysis vintage over 3 months).

Intervention: IDPN (Olimel N12, Baxter, 1L/session) or regular care without IDPN.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age above 18 years
  • •Receiving HD treatment over 3 months
  • •Receiving HD treatment 3 times per week for at least 4 hours per session
  • •24-hour urine production < 100 mL
  • •Adequate dialysis dose (eKt/V over 1.2)
  • •AV fistula with blood flow (measured invasively or by Doppler ultrasound) over 750 mL/min

Exclusion Criteria

  • •Occurrence of intradialytic hypotension in the last month, defined by systolic blood pressure < 90 mm Hg combined with a nursing intervention
  • •Hospitalization < 3 months before inclusion
  • •Active infection or inflammation at randomization
  • •Use of oral or intravenous corticosteroids
  • •Incapacitation
  • •Patients who are not expected to be able to complete the study protocol (e.g., due to a planned kidney transplantation within the planned study time frame)
  • •Pregnancy
  • •Use of oral anticoagulants or antiplatelet agents that cannot be safely stopped during the study
  • •Diabetes mellitus
  • •AV fistula with recirculation

Arms & Interventions

intra dialytic parenteral nutrition (Olimel N12, Baxter, 1L/session)

Experimental

intra dialytic parenteral nutrition (Olimel N12, Baxter, 1L/session)

Intervention: intra dialytic parenteral nutrition (Olimel N12, Baxter, 1L/session) (Dietary Supplement)

Control

No Intervention

no intervention according to usual care

Outcomes

Primary Outcomes

Myofibrillar fractional synthetic rate

Time Frame: At baseline and during the first dialysis sessions in the following two weeks.

Difference in myofibrillar fractional synthetic rate during treatment with IDPN versus usual care

Secondary Outcomes

  • Forearm amino acid (AA) balance(During the first visit in intervention and cross-over usual care regiment.)
  • Intradialytic blood pressure and cardiac output(Cardiac output will be measured at baseline and during the first dialysis sesions in the following 2 weeks. Predialysis systolic blood pressure, intradialytic blood pressure decrease, and ultrafiltration volume will be measured at each dialysis session.)
  • Amino acid loss in dialysate(Amino acid loss in dialysate will be measured during V2 and V5.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Wesley Visser

Principal investigator, PhD, RD

Erasmus Medical Center

Study Sites (1)

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