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Balance Study on ICU-acquired Hypernatremia and Sodium Handling (BIAS)

Balance Study on ICU-acquired Hypernatremia and Sodium Handling

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03093766
Acronym
BIAS
Enrollment
155
Registered
2017-03-28
Start date
2017-08-07
Completion date
2018-06-01
Last updated
2018-07-18

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

Conditions

ICU-acquired Hypernatremia

Keywords

Aetiology

Brief summary

The goal of this study is to find differences between patients who do and do not develop ICU-acquired hypernatremia (IAH). Therefore extended sodium and fluid balances will be performed. Also a couple of other factors that possibly contribute to the development of IAH and/or could give clues about the mechanisms in the development of IAH will be investigated.

Detailed description

ICU-acquired hypernatremia (IAH) is common in critically ill patients, but it's aetiology is still not fully understood. Sodium overload and inadequate fluid administration are generally considered important factors, but a previous retrospective study did not reveal differences in sodium or fluid balances between patients who did and did not develop IAH. Because this was retrospective these balances will be prospectively studied in this study to be more sure about the importances of these balances in the development of IAH. Previous studies indicated that (a lot) more factors contribute to the development of IAH. In this study these factors will be investigated, hoping to find differences between patients who do and do not develop IAH.

Interventions

None listed

Sponsors

University Medical Center Groningen
CollaboratorOTHER
Frisius Medisch Centrum
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Predicted duration of ICU-admission \>48 hours

Exclusion criteria

* Renal replacement therapy * Reason for admission necessitates actively elevation of serum sodium concentration * Electrolyte disturbance as reason for admission * ICU re-admission within 30 days * Referral from another ICU * Serum sodium concentration on admission 143mmol/l or above

Design outcomes

Primary

MeasureTime frameDescription
Sodium balanceDuring ICU-admissionDifferences in sodium balances between patients who do and do not develop IAH
Fluid balanceDuring ICU-admissionDifferences in fluid balances between patients who do and do not develop IAH

Secondary

MeasureTime frameDescription
Kidney functionDuring ICU-admissionDifferences in parameters concerning kidney function (creatinine, urea) between patients who do and do not develop IAH
InflammationDuring ICU-admissionDifferences in inflammation (CRP, infections) between patients who do and do not develop IAH
Nutritional stateDuring ICU-admissionDifferences in nutritional state (albumin, BIVA-measurement) between patients who do and do not develop IAH

Countries

Netherlands

Outcome results

None listed

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