Actively Recruiting

Age: 18Years +
All Genders
ID06646484

Interest of Impedancemetry in Monitoring Hydration and Hyponatremia During Subarachnoid Hemorrhages

Led by Hospices Civils de Lyon · Updated on 2025-01-13

100

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Subarachnoid hemorrhage (SAH) is a serious and rare type of stroke caused mainly by the rupture of an intracranial aneurysm, leading to bleeding in the meningeal spaces. One significant late complication is delayed cerebral ischemia (DCI), which causes new neurological problems. To prevent issues related to blood volume changes, especially hyponatremia, it is important to carefully evaluate water and sodium balance, which is challenging using only indirect clinical and biological measures. This study evaluates the use of impedancemetry, a diagnostic test that measures body water volumes and sodium load, to help manage hydration and sodium levels in patients with SAH. Each participant will receive repeated impedancemetry measurements during their hospital stay in addition to standard care. These measurements will be compared to usual hydration and sodium tests, and the agreement with clinical status will be assessed. Participants will be monitored every 48 hours during their average 21-day stay in the neurological intensive care unit. Researchers will measure hydration levels and monitor sodium balance through repeated assessments. The study focuses on how impedancemetry can assist in the ongoing management of hydration and hyponatremia in this patient group, with careful tracking throughout their hospital course.

CONDITIONS

Official Title

Interest of Impedancemetry in Monitoring Hydration and Hyponatremia During Subarachnoid Hemorrhages

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult man or woman
  • Hospitalized following Subarachnoid Hemorrhage within 72 hours of bleeding
  • Admitted to the neurological intensive care unit for less than 48 hours
  • Able to understand the ins and outs of the study
  • Has expressed non-opposition to participate
Not Eligible

You will not qualify if you...

  • Patients under legal protection
  • Pregnancy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospices Civils de Lyon. Neurological ICU

Lyon, France, France, 69500

Actively Recruiting

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Research Team

T

Thomas RITZENTHALER, MD

J

Julien BERTHILLER

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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