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Sodium Management in Acute Neurological Injury

Sodium Management in Patients With Acute Neurological Injury

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01558843
Acronym
SANI
Enrollment
400
Registered
2012-03-20
Start date
2012-02-01
Completion date
2016-10-01
Last updated
2019-05-01

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

Conditions

This Study is to Understand the Current Practice of Sodium Management in Acute Neurological Injury

Keywords

Sodium Management, Neurointensive Care, Hyponatremia

Brief summary

This multicenter, observational, study will enroll severe neurologically injured patients both prospectively and retrospectively. The aims are to identify the percent of neurocritical care patients with sodium levels ≤ 135 mEq/L, describe treatment strategies employed, determine the correlation of clinical factors (i.e. GCS, ICP) with serum sodium concentrations in patients prior to sodium altering therapy, and evaluate outcomes through evaluation of length of stay, discharge disposition, and modified Rankin score (mRS).

Interventions

None listed

Sponsors

Astellas Pharma Inc
CollaboratorINDUSTRY
Washington University School of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* age ≥ 18 years of age * admitted to an intensive care unit for more than 48 hours * ICD-9 codes for aneurysmal SAH, TBI, IPH, or intracranial tumor.

Countries

United States

Outcome results

None listed

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