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Ketoacid Analogues Intradialytic Effect on Inflammation

Effect of Intradialytic Administration of Ketoacid Analogues on Inflammatory Parameters in Patients Undergoing Chronic Hemodialysis Twice a Week

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06392516
Enrollment
86
Registered
2024-04-30
Start date
2024-04-29
Completion date
2024-09-30
Last updated
2024-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodialysis Complication

Keywords

ketoacid analogues, inflammation, hemodialysis

Brief summary

this study tries to measure the effect of intradialytic ketoacid analogues on inflammatory parameters

Detailed description

this study will measure inflammation parameters: * interleukin 6 * malnutrition inflammation score * neutrophil lymphocyte ratio * monocyte lymphocyte ratio * thrombocyte lymphocyte ratio the duration of intervention is 12 weeks

Interventions

DRUGKetoacid

250 ml ketoacid two hours before the hemodialysis session ended

Sponsors

RSUP Fatmawati
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

intervention and control

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patient who undergo hemodialysis two times a week

Exclusion criteria

* travelling hemodialysis * acute conditions * HIV patient * acute infection * stroke and immobilized patient

Design outcomes

Primary

MeasureTime frameDescription
interleukin-612 weeksin pg/mL, no limit values
malnutrition inflammation score12 weeksconsists of ten components, based on subjective complaints combined with albumin serum (in g/dL), serum iron (in micromol/L, and total iron binding capacity (in micromol/L). the sum of all components \>5 means have high inflammation status
neutrophil lymphocyte ratio12 weeksthe percentage ratio of neutrophil count and lymphocyte count will be combined to neutrophil lymphocyte ratio
monocyte lymphocyte ratio12 weeksthe percentage ratio of monocyte count and lymphocyte count will be combined to monocyte lymphocyte ratio
thrombocyte lymphocyte ratio12 weeksthe percentage ratio of thrombocyte (in per microliter of blood) and lymphocyte count will be combined to thrombocyte lymphocyte ratio

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026