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Optimalisation of the Treatment of Acute Neonatal Hyperammonaemia

Optimalisation of the Treatment of Acute Neonatal Hyperammonaemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05754372
Enrollment
10
Registered
2023-03-03
Start date
2023-01-15
Completion date
2026-12-31
Last updated
2024-04-15

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

Conditions

Hyperammonemic Encephalopathy

Keywords

hemodialysis, neonate, Hyperammonemic Encephalopathy, inborn error of metbolism

Brief summary

Acute neonatal hyperammonemia is associated with poor neurological outcomes and high mortality. A user-friendly and widely applicable algorithm - based on kinetics - to tailor the treatment of acute neonatal hyperammonemia. A single compartmental model was calibrated assuming a distribution volume equal to the patient's total body water (V), as calculated using Wells' formula, and dialyzer clearance as derived from the measured ammonia time-concentration curves during 11 dialysis sessions in four patients (3.2 +/- 0.4 kg). Based on these kinetic simulations, dialysis protocols could be derived for clinical use with different body weights, start concentrations, dialysis machines/dialyzers and dialysis settings (e.g., blood flow QB). By a single measurement of ammonia concentration at the dialyzer inlet and outlet, dialyzer clearance (K) can be calculated as K = QB\[(Cinlet - Coutlet)/Cinlet\]. The time (T) needed to decrease the ammonia concentration from a predialysis start concentration Cstart to a desired target concentration Ctarget is then equal to T = (-V/K)LN(Ctarget/Cstart). By implementing these formulae in a simple spreadsheet, medical staff can draw an institution-specific flowchart for patient-tailored treatment of hyperammonemia. The aim of this study is to validate these formula with a prospective study.

Interventions

DIAGNOSTIC_TESTuser-friendly and widely applicable algorithm to tailor the treatment of acute neonatal hyperammonemia

user-friendly and widely applicable algorithm to tailor the treatment of acute neonatal hyperammonemia, based on kinetic modelling

Sponsors

University Hospital, Ghent
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 1 Years
Healthy volunteers
No

Inclusion criteria

* severe acute neonatal hyperammonaemia for which acute hemodialysis is indicated * inborn error of metabolism * below 1 year of age

Exclusion criteria

* older than 1 year

Design outcomes

Primary

MeasureTime frameDescription
serum ammonium levels1 yearserum ammonium levels

Secondary

MeasureTime frameDescription
Removal of treatment sodium benzoate, L-arginine1 yearserum and dialysate concentration (mg/dL) of sodium benzoate and L-arginine

Countries

Belgium

Contacts

Primary ContactEvelien Snauwaert, MD, PhD
evelien.snauwaert@uzgent.be00 32 9 332 69 05
Backup ContactSunny Eloot, PhD
sunny.eloot@ugent.be00 32 9 332 10 25

Outcome results

None listed

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