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Nephrogenic Diabetes Insipidus During Prolonged Sevoflurane Sedation in the ICU: a Retrospective Analysis

Incidence of Nephrogenic Diabetes Insipidus During Prolonged Sevoflurane Sedation in the Intensive Care Unit: a Retrospective Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04939753
Enrollment
1000
Registered
2021-06-25
Start date
2021-05-26
Completion date
2023-04-01
Last updated
2023-04-27

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

Conditions

Nephrogenic Diabetes Insipidus

Brief summary

The investigators aim to retrospectively explore the electronic medical records of all patients who were admitted to the Intensive Care Unit (ICU) of the UZ Brussels in the last 10 years (March 1st 2011- March 1st 2021) and who received prolonged sedation (\>24h) with sevoflurane.

Interventions

DRUGSevoflurane

Sevoflurane administration to sedate the patient

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Sevoflurane administration \>24h * 18 years and older

Exclusion criteria

* \< 18 years old * Pre-existing diabetes insipidus * Use of drugs at risk for diabetes insipidus (including lithium, cisplatin) * Hypercalcemia (persistently \>2.75 mmol/L) * Pituitary or acute brain surgery * Patients requiring continuous renal replacement therapy * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Nephrogenic Diabetes Insipidus prevalenceup to 8 weeksHow many patients under sevoflurane sedation ultimately develop NDI? NDI confirmed by demonstrating the absence of a urine concentrating response to exogenous Arginine Vasopressine.

Secondary

MeasureTime frameDescription
Number of symptoms of NDIup to 8 weeksNumber of symptoms of NDI do these patients show?
Number of patients with an abnormal physical examination.during hospitalization, up to 8 weeks.Typical physical symptoms of (N)DI: tired, lethargic, tachycardia, tachypnea, hypotension and dry mucous membranes.
Number of patients with urine with an abnormal osmolalityduring hospitalization, up to 8 weeks.Lab testing of urine: osmolality \< 300 mosm/kg
Number of patients with electrolyte abnormalities as assessed by lab results.during hospitalization, up to 8 weeks.Lab results of hematology and chemistry labs show an electrolyte imbalance.
Number of patients that have an abnormal abdominal echo of the bladder.during hospitalization, up to 8 weeks.Echo shows an enlarged bladder.
Amount of time patient was placed under sevoflurane sedation.up to 8 weeksHow long are they under sevoflurane sedation.
Number of patients with excessive urine outputduring hospitalization, up to 8 weeks.Amount of urine output: \>40 ml/kg/24h
Number of patients that show an abnormal amount of fluid intakeduring hospitalization, up to 8 weeks.\>2.5l/day
Timing of symptoms of NDIup to 8 weeksAfter how much time do these patients show symptoms of NDI?
Number of patients that develop risk factors of NDIup to 8 weeksNumber of patients that develop risk factors (electrolyte disorder, urinary obstruction) for NDI.

Countries

Belgium

Outcome results

None listed

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