Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT05148208 |
| Other study ID # |
202100665 |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
January 1, 2022 |
| Est. completion date |
July 1, 2022 |
Study information
| Verified date |
November 2021 |
| Source |
University Medical Center Groningen |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
We perform a pilot study to investigate whether intra-dialytic creatine supplementation via
the dialysate will result in higher intra-erythrocyte creatine concentrations. Secondary
outcomes will include changes in muscle mass, muscle strength and cognition.
Description:
Dialysis is a life-saving treatment, but unfortunately health-related quality of life (HRQoL)
of dialysis patients is poor and mortality risks are high compared to the general population.
Although several potentially modifiable (e.g. pre-dialysis care and nutritional status) and
unmodifiable risk factors (e.g. age and genetics) for excess risk of mortality and poor HRQoL
have been identified in dialysis-dependent patients with chronic kidney disease (CKD), there
is great need for identification of new potentially modifiable risk factors. We hypothesize
that creatine deficiency is such a modifiable risk factor, which underlies several important
causes for impaired HRQoL hemodialysis patients, such as protein energy wasting (PEW),
sarcopenia, fatigue, muscle weakness, depression, cognitive impairment, and increased
susceptibility and a higher risk of an adverse course of infectious diseases. We propose that
creatine supplementation is particularly important for patients with dialysis-dependent CKD
because (1) endogenous synthesis of creatine in these patients is severely impaired due to
the virtual absence of kidney function and, consequently, the virtual absence of the first
enzymatic step required for endogenous absence of creatine from the amino acids arginine and
glycine (2) unopposed losses of creatine to the dialysis fluid during dialysis sessions, and
(3) inadequate intake of creatine due to advices towards a primary plant-based diet in these
patients. All this comes on top of the normally existing continuous non-enzymatic conversion
of approximately 1.6-1.7% of the endogenous creatine pool to creatinine, which necessitates
continuous replenishment of creatine by the combination of endogenous synthesis and dietary
intake to remain in steady-state. This is a novel understanding because until recently it was
not recognized that kidney function is an important contributor to endogenous creatine
synthesis, so that the capacity to of patients with dialysis-dependent CKD to maintain
creatine homeostasis in the light of ongoing conversion of creatine into creatinine,
additional unopposed losses of creatine to the dialysis fluid and an inadequate dietary
intake is severely impaired. Patients with dialysis-dependent CKD could benefit from creatine
supplementation by allowing for maintenance of their endogenous creatine pools, which would
help them to sustain bodily functions which depend on creatine availability, including normal
function of muscles, heart, the immune system and brain.
Based on these novel/ recent findings, we hypothesize that creatine, intradialytic creatine
supplementation may help to maintain creatine homeostasis among dialysis-dependent chronic
kidney disease patients, and consequently improve muscle status, nutritional status,
neurocognitive status fatigue and HRQoL.
Objective: The primary objective of this pilot study is the feasibility of prolonged
intra-dialytic creatine supplementation.
The secondary objectives of this pilot study are to study the safety of prolonged
intra-dialytic creatine supplementation for dialysis patients and finding the optimal dosage
to replenish the creatine pool, to this end we will step wisely increase creatine
concentrations of the dialysis solution (in the range of 0.5 mM to a maximum of 2mM, with the
latter reflecting the concentration that can be reached after an oral bolus of creatine).
The third objective is to obtain pilot data on the effect of intradialytic creatine
supplementation on muscle status, nutritional status, neurocognitive status fatigue and HRQoL
to allow for calculation of the power for a lager intervention study.
Study design: Block-randomized double-blind placebo-controlled pilot study in 16 hemodialysis
patients (which will be divided into four groups (0.5mM, 1.0mM, 1.5mM, 2.0mM) each consisting
of three patients receiving creatine and one receiving placebo). The total study duration is
8 weeks with 6 weeks of active treatment and 2 weeks of wash-out.
Study population: The study population comprises of a total of 16 adult (≥18 years)
clinically stable patients with dialysis-dependent chronic kidney disease treated by
conventional hemodialysis in the UMCG and the Dialysis Center Groningen Intervention:
Creatine will be added to the dialysis fluid and will thus be continuously administered
during the whole hemodialysis session. We will study the effect of four increasing dosages of
creatine (3 out of 4 patients per block) or placebo (1 out of 4 patients per block) in four
groups of four patients: 0.5mM, 1.0mM, 1.5mM, or 2.0mM of creatine. The patients will receive
creatine supplementation or placebo (sterile water with the same composition as the
dialysate) during each hemodialysis session during a total period of 6 weeks.
Creatine-monohydrate, Creapure® "Pharma Quality" (not GMP), produced by AlzChem Trostberg,
Germany will be used for preparation of a 50 mmol/L stock solution of creatine which will be
added to the dialysis fluid to reach the projected dialysate concentrations.
Main study parameters/endpoints: The main parameters for the pilot study are the plasma
creatine concentration and intra-erythrocytic creatine concentration of both pre- and
post-hemodialysis samples. Intra-erythrocytic creatine concentration will be used as a
non-invasive proxy for creatine tissue uptake. Secondary study parameters are hand grip
strength as a measure of muscle strength, the combined interdialytic urinary and
intradialytic dialysate excretion of creatinine as a measure of muscle mass, and
bioelectrical impedance analysis (BIA) as a measure of body composition and nutritional
status. Other study parameters are N-terminal pro-brain natriuretic peptide (NT-proBNP) as a
cardiac function marker, high sensitivity troponin T (hs-TNT) as a cardiac ischaemia marker,
C-reactive protein as an inflammation marker, self-reported physical health using the EQ-6D,
SF36, and the DSI, fatigue using the CIS and cognitive functions using the CFQ.
Nature and extent of the burden and risks associated with participation, benefit and group
relatedness: For this study, during each of study visits (baseline, week 3, week 6, and after
a wash-out period of 2 weeks) patients will have to stay at the dialysis unit for 45 minutes
longer than usual for their regular HD treatment. Besides arterial blood sampling (from the
dialysis line) no venepunctures are necessary. For each study visit the total blood volume
will not exceed 152 ml. Participants with a residual diuresis of ≥ 200 ml per 24h are asked
to collect interdialytic urine. During the hemodialysis session, the complete dialysate
volume will be collected in a tank. Dialysate is considered a 'waste product' and the
collection of dialysate is no burden for the patient. Questionnaires can be filled in during
the hemodialysis session. None of the health tests performed as part of this study cause
physical discomfort. To minimize any risk of falling, physical tests are performed prior to
the dialysis session and under the supervision of an investigator. We believe it is justified
to perform the proposed study in order to elucidate the possible effects of intra-dialytic
creatine supplementation on e.g. muscle status, nutritional status, neurocognitive status
fatigue in hemodialysis patients. The finding of a beneficial effect will improve HRQoL and
mortality rates.
