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Recruiting NCT06646484

Interest of Impedancemetry in Monitoring Hydration and Hyponatremia During Subarachnoid Hemorrhages

Observational Subarachnoid Hemorrhage (SAH)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Impedancemetry evaluation.
Who it may be relevant to
Registry conditions: Subarachnoid Hemorrhage (SAH). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Subarachnoid hemorrhage (SAH) is a rare and serious form of stroke, mainly linked to the rupture of an intracranial aneurysm responsible for bleeding into the meningeal spaces. The main late serious complication is delayed cerebral ischemia (DCI), resulting in the appearance of new neurological deficits. Prevention of ICR involves in particular maintaining euvolemia, and early treatment of hyponatremia, itself dependent on the level of volume. Evaluation of water status and sodium balance is therefore essential. This assessment is complicated and relies on indirect parameters, both clinical and biological. Impedancemetry, making it possible to measure water volumes and sodium load, could be an aid in the management of blood volume and sodium intake.

Interventions

  • Diagnostic test Impedancemetry evaluation
    Each patient eligible for the study will, additionally to the standard care, have repeated measure of impedancemetry along their hospital stay ; Theses measure will be compared to the usual measure of hydration and natremia and agreement between clinical status of interest will be discussed.

Primary outcome measures

  • Hydration measurements [Time frame: Every 48 hours during the mean 21 days of stay in the neurological ICU.]

Eligibility criteria

Inclusion criteria

  • Adult man, woman
  • Hospitalized following Subarachnoid Hemorrhage within 72 hours of bleeding
  • Admitted to the neurological intensive care unit for less than 48 hours
  • Being able to understand the ins and outs of the study
  • Having expressed his non-opposition

Exclusion criteria

  • Patients under legal protection
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Hospices Civils de Lyon. Neurological ICU — Lyon

Identifiers

NCT: NCT06646484 · 69HCL24_0783 · 2024-A02117-40

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗