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Evaluation of Volume and Electrolyte Balance in Hyponatremia Treatment - a Prospective Observational Trial

Evaluation of Volume and Electrolyte Balance in Hyponatremia Treatment - a Prospective Observational Trial (EvenT)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05692726
Acronym
EvenT
Enrollment
50
Registered
2023-01-20
Start date
2022-10-15
Completion date
2026-09-30
Last updated
2025-09-11

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

Conditions

Non-hypervolemic Hyponatremia

Keywords

Electrolyte-free water clearance, hyponatremia

Brief summary

To assess quantitatively the evolution over time of electrolyte-free water clearance and electrolyte mass balance in patients with non-hypervolemic hypotonic hyponatremia

Detailed description

Achieving recommended treatment targets in management of hyponatremia is challenging: plasma sodium must be increased effectively but, at the same time, overcorrection has to be prevented. Yet, predictors of change of sodium over time have not been delineated properly. It was found, that evidence hinting to the fact that sodium baseline itself is crucial with respect to sodium evolution. The goal of this study is to gather prospective data in order to precisely delineate the role of initial sodium levels by correlating those to plasma sodium evolution and electrolyte free water evolution. It is aimed to decipher patterns of sodium evolution with respect to anthropometric data, such as body composition analyses and blood pressure and markers of innate regulation mechanisms of body volume like aldosterone and renin. In addition, apart from these clinical aspects, a better appreciation of the physiological responses to hyponatremia treatment in terms of water and electrolyte balances is undoubtedly necessary to improve understanding of the body's mechanisms involved in osmotic homeostasis and cell volume control. Since studies to date also lack consideration of the intracellular department, the aim is to close that gap.

Interventions

OTHERPatients

Patients will get study-specific measurements within first 5 days of standard of care treatment of hyponatremia or until discharge

Sponsors

University of Cologne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Adult patients ≥ 18 years * Hypotonic hyponatremia * glucose-corrected plasma sodium \<130 mmol/l * serum osmolality \<280 mosmol/kg or lack of signs of non-hypotonic hyponatremia

Exclusion criteria

* Signs of extracellular volume expansion * Patients with liver cirrhosis and severe liver damage AST/ALT\>3xULN, AP\>6xULN, Bilirubin ≥ 3mg/dl * Patients with heart failure * Patients on dialysis and/or patients with oliguric renal impairment and plasma creatinine ≥ 3mg/dl * Patients after organ transplantation

Design outcomes

Primary

MeasureTime frameDescription
Changes in Plasma Sodiumbaseline, every day up to 30 daysMeasurement of plasma sodium in blood samples
Changes in plasma osmolalitybaseline, every day up to 30 daysMeasurement of plasma osmolality for determination of electrolyte-free water clearance before, during and after hyponatremia treatment
Changes in urine osmolalitybaseline, every day up to 30 daysDetermination of electrolyte-free water clearance before, during and after hyponatremia treatment by measurement of urine osmolality
Changes in urine volumebaseline, every day up to 30 daysDetermination of electrolyte-free water clearance before, during and after hyponatremia treatment by measurement of urine volume

Secondary

MeasureTime frameDescription
Changes in blood pressurebaseline, every day up to 30 daysMeasurement of blood pressure before, during and after hyponatremia treatment
Changes in cell sizebaseline, every day up to 30 daysDetermination of blood cell size via measurement of mean corpuscular volume
Changes in intracellular electrolyte levelsbaseline, every day up to 30 daysMeasurement of whole blood samples via ICP-mass spectrometry
Changes in body weightbaseline, every day up to 30 daysMeasurement of body weight before, during and after hyponatremia treatment by bioimpedance measurement
Changes in renin levelsbaseline, every day up to 30 daysMeasurement of renin in blood samples
Changes in aldosterone levelsbaseline, every day up to 30 daysMeasurement of aldosterone in blood samples
Changes in copeptin levelsbaseline, every day up to 30 daysMeasurement of copeptin in blood samples
Changes in total body waterbaseline, every day up to 30 daysMeasurement of body water before, during and after hyponatremia treatment by bioimpedance measurement
Changes in intracellular volumebaseline, every day up to 30 daysMeasurement of intracellular volume before, during and after hyponatremia treatment by bioimpedance measurement
Changes in extracellular volumebaseline, every day up to 30 daysMeasurement of extracellular volume before, during and after hyponatremia treatment by bioimpedance measurement

Countries

Germany

Contacts

Primary ContactVolker Burst, MD, Prof
volker.burst@uk-koeln.de+49 221-478-97222
Backup ContactSadrija Cukoski
sadrija.cukoski@uk-koeln.de

Outcome results

None listed

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