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NCT Number: NCT06498856

Saline Infusion Test in Hyponatremia

Observational study of biochemical volume biomarker levels in response to a standardized intravenous isotonic saline infusion in patients with hyponatremia.

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Key information

About this study

Hyponatremia (low plasma sodium concentration) is a common electrolyte disorder among hospitalized patients that can lead to complications such as gait instability, falls and mental changes. Both hyponatremia itself and overly rapid correction of hyponatremia may lead to brain damage.

There are several underlying causes of hyponatremia that require different treatment strategies. Specifically, hypovolemia is treated with fluid infusion while other common causes such as the syndrome of inappropriate diuresis (SIAD) and hypervolemic conditions need fluid restriction. In clinical practice, it can be challenging to identify the main cause of hyponatremia due to overlapping diagnosis and unreliable diagnostic tools, typically leading to a timely trial and error approach to therapy.

A saline infusion test (SIT) is often used to diagnose hypovolemic hyponatremia. To our knowledge, the test has never been validated, but relies on the rationale that the sodium concentration will increase more with saline infusion in hypovolemia than in other causes of hyponatremia. Typically, one liter of isotonic saline is infused intravenously and an arbitrarily set cut-off for sodium increase is used to indicate hypovolemia. As the response of sodium depends on several factors that affects the renal free water excretion capacity, this measure may not be the most accurate nor the most efficient. Another, more direct, approach could be to measure the change in biochemical markers of circulating volume in response to the volume expansion that comes with saline infusion. We will measure several different biomarkers before, during and after a standardized isotonic saline infusion in patients hospitalized with hyponatremia. Based on the results, we hope to develop a more precise tool for the differential diagnosis of hyponatremia.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Plasma sodium 120-130 mmol/L
  • Effective osmolality (2 x plasma sodium + plasma glucose) < 275 milliosmol/L
  • Age > 18 years

Exclusion criteria

  • Intensive care unit (ICU) admission
  • Adequate sodium correction rate: > 4 mmol/L last 24 hours
  • Primary polydipsia: urine osmolality < 100 mOsm/L
  • Hypertonic saline therapy
  • Adrenal insufficiency
  • Severe heart failure: ejection fraction < 35 % or clinical suspicion of decompensated heart failure
  • Ascites grade 3 (marked abdominal distention and discomfort)
  • Chronic renal failure stage 4 or 5: estimated glomerular filtration rate < 30
  • Failure to submit informed consent

Treatment and study plan

isotonic saline infusion

Other

Volume expansion with one liter of isotonic saline intravenously over two hours.

Primary outcomes

  1. Copeptin plasma levels

    Time frame: 240 minutes

    Changes in copeptin levels in response to isotonic saline infusion

Study contacts

Contact information is provided by the study sponsor or research team.

Kaja Grønning, MD

CONTACT

[email protected]

67960000

Sponsors and collaborators

Lead sponsor

University Hospital, Akershus

Other

Collaborators

  • Hormone Laboratory, Aker University Hospital, Oslo, Norway

Registry information

Acronym: SITH

Important dates

Study start
2024
Primary completion
2025
Study completion
2028
First posted
Jul 12, 2024
Registry last updated
Jul 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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