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HyponatremiaNCT07430787

Hyponatremia - Complications, Prognosis, Epidemiology in Finnish Tertiary Care

An observational study of Hyponatremia and Osmotic Demyelination Syndrome, run by University of Turku at 1 site in Finland.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Study Objectives and Hypothesis To determine the incidence of hyponatremia at TYKS and the factors associated with it. To assess how rapidly hyponatremia was corrected and how the rate of correction affected patient prognosis. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
10,000 participants
Where
1 siteFinland
Study dates
1 Sep 2023to 31 Dec 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The study design was to enroll as general population that are hospitalized as possible. From this population the main focus group of hyponatremia and ODS patients were selected and formed case-control groups.

Who may be able to join

  • Two sodium measurements in Tyks laboratories between 12-36 hours.

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Finland1 site
  • University of Turku

    Turku, Southwest Finland, 20300

Other trials in Finland

About this study

Official title: Clinical Significance of Hyponatremia

Study Objectives and Hypothesis

To determine the incidence of hyponatremia at TYKS and the factors associated with it.

Read more

To assess how rapidly hyponatremia was corrected and how the rate of correction affected patient prognosis.

To evaluate treatment modalities and their impact on patient prognosis, length of hospital stay, and their appropriateness in comparison with national and international treatment guidelines.

To determine the incidence of osmotic demyelination at TYKS and the factors associated with it.

To assess other complications and their clinical significance.

To evaluate the impact of hyponatremia on various endpoints, such as mortality, length of hospital stay, seizures, confusion, and similar outcomes.

Read the detailed description

Clinical Significance of Hyponatremia (Study Protocol)

Investigators: Tyko Hellsten, Anssi Mustonen, Ilpo Nuotio

Background of the Study General Background

Hyponatremia is a common electrolyte disorder occurring in approximately 15-30% of hospitalized patients (3,4). Most cases are mild and minimally symptomatic. The most clinically significant cases are rapidly developing severe hyponatremia, which may cause neurological emergencies and death, and chronic severe hyponatremia, in which overly rapid correction may lead to permanent neurological injury and, in the most severe cases, death (3,4). Hyponatremia is not an independent disease but a consequence of underlying illnesses, adverse drug effects, inappropriate fluid therapy, or, rarely, lifestyle-related factors.

Hyponatremia is classified as mild when serum sodium is 130-134 (-138) mmol/L. Although mild hyponatremia has been associated with increased hospital visits, prolonged hospital stays, sarcopenia, falls, fractures, and increased mortality, it is not typically an active target of treatment, and there are no reports on the effectiveness of its treatment.

Rapidly developing severe hyponatremia presenting with neurological symptoms, cerebral edema, or seizures requires an initial rapid increase in serum sodium followed by slower correction (1). In chronic severe hyponatremia, correction must be slow from the beginning to avoid neurological complications (1). Since the rate of development is often unknown, practical guidance recommends an initial rapid increase of 5-6 mmol/L in patients with neurological symptoms, while sodium should be corrected slowly in minimally symptomatic patients.

Hyponatremia is also classified according to serum osmolality into pseudo-, hypertonic, isotonic, and hypotonic hyponatremia. Pseudohyponatremia and hypertonic/isotonic hyponatremia are most commonly caused by hyperglycemia or, rarely, by fluids used in operative settings. This study focuses on hypotonic hyponatremia, its prevalence, associated diseases, clinical significance in acute care, and treatment.

Classification, Etiology and Diagnostics

Hyponatremia is classified as:

Mild: 130-134 (-138) mmol/L

Moderate: 120 (-125) to 130 mmol/L

Severe: <120-125 mmol/L (1)

Based on duration:

Acute hyponatremia develops within 48 hours (e.g., postoperative fluid therapy with increased ADH secretion, polydipsia in psychiatric patients or endurance athletes) (1,3,4).

Chronic hyponatremia develops over more than 48 hours, has an unclear duration, or develops outside hospital settings (1,3,4).

Based on volume status, hypotonic hyponatremia is classified as:

Hypovolemic

Euvolemic

Hypervolemic

Hypovolemic hyponatremia presents with clinical signs of dehydration and is caused by gastrointestinal losses or renal losses (e.g., diuretics, mineralocorticoid deficiency) (4).

Euvolemic hyponatremia, the most common type, is often due to SIADH (syndrome of inappropriate antidiuretic hormone secretion), associated with medications, stress, CNS and pulmonary diseases, and malignancies. Other causes include hypothyroidism, adrenal insufficiency, and abnormal dietary habits (4).

Hypervolemic hyponatremia results from decreased effective arterial blood volume, leading to reactive water retention (4), as seen in liver cirrhosis, heart failure, nephrotic syndrome, and polydipsia.

Assessment of vasopressin activity is commonly based on the urine-to-serum osmolality ratio (U-osmolality > S-osmolality or U-osmolality 100-300) (6), since direct vasopressin measurement is unreliable and copeptin is not routinely used.

Treatment and Associated Risks

Treatment depends on the rate of onset, symptom severity, and etiology. Current guidelines are largely consistent.

If there is a high risk of osmotic demyelination syndrome (ODS) (Na <105 mmol/L, alcoholism, hypokalemia, malnutrition, liver disease), correction should not exceed 4-6 mmol/L per 24 hours (3). Otherwise, up to 8 mmol/L in the first 24 hours is considered safe. In confirmed acute cases (<24-48 hours), correction may proceed more rapidly (3).

Rapid-onset hyponatremia causes cerebral edema due to water movement into brain cells (4). Chronic hyponatremia allows osmotic adaptation, reducing cellular swelling (4).

Known intracranial pathology increases herniation risk, and hypertonic 3% saline should be considered early (1). Sodium levels should be monitored every 4-6 hours, or hourly in severe cases (3).

In Finland, national acute care guidelines recommend fluid restriction for slowly developing, mildly symptomatic hyponatremia. Hypertonic 3% saline is reserved for severe neurological symptoms (8).

After acute correction, hyponatremia may not require further specific treatment if the underlying cause has been addressed. SIADH is often chronic; first-line treatment is fluid restriction and correction of underlying causes (4). Tolvaptan is rarely used due to cost and limited reimbursement. Oral sodium chloride may be considered in SIADH if fluid restriction is insufficient (1).

Complications and Prognosis

Hyponatremia is the most common cause of ODS, particularly in chronic cases with overly rapid correction (2). Clinical manifestations include central pontine and extrapontine myelinolysis (2). Symptoms range from dysarthria and dysphagia to spastic tetraparesis and extrapyramidal features.

MRI is essential in diagnosis. Imaging findings do not directly correlate with prognosis (2).

There is no specific treatment for ODS; prevention through cautious correction is key (1,3). Prognosis has improved substantially compared to the 1980s (2).

Study Objectives and Hypotheses

To determine the incidence of hyponatremia and associated factors at TYKS (Turku University Hospital).

To evaluate correction rates and their impact on prognosis.

To assess treatment modalities, hospital length of stay, outcomes, and adherence to guidelines.

To determine the incidence and risk factors of ODS at TYKS.

To identify other complications and their significance.

To evaluate the impact of hyponatremia on mortality, hospital stay, seizures, confusion, and other endpoints.

The first study will assess incidence and associated factors (2016-2020). The second will evaluate sodium levels and mortality across diagnosis groups. The third will assess ODS incidence and associated factors. The fourth will focus on management of severe hyponatremia.

Materials and Methods

A registry-based study will include all patients with hyponatremia and all cases of osmotic demyelination syndrome treated at TYKS between January 1, 2016, and December 31, 2020.

Data will be analyzed using statistical software (SAS, SPSS, R) by study investigators.

Results will be published in international medical journals and presented at national and international conferences.

Significance of the Study

Hyponatremia is a common clinical challenge in emergency and inpatient care. Controlled correction requires monitored care. This study aims to clarify:

At which sodium levels monitored correction is necessary

What constitutes a safe correction rate

The frequency of complications with rapid correction

Whether patients are overtreated

The impact of hyponatremia and comorbidities on prognosis and mortality

The goal is to clarify diagnostic and therapeutic strategies for hyponatremia.

Ethical Considerations

This is a registry-based study. Separate ethical approval is not required. Data will be anonymized before analysis.

Study Timeline

Study planning: from January 1, 2022 Research permits and data retrieval: from May 1, 2022

Keywords
hyponatremia, epidemiology, Osmotic Demyelination Syndrome, Alchol use disorder
Medical subject headings
Hyponatremia, Alcoholism

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence of ODS in hyponatremia patients

    The primary variable is dichotomous. It is defined based on radiologists' reports and confirmed by an expert panel.

    Measured: From enrollment to the end of the treamtent period. Usually 2-21 days.

  2. Osmotic demyelination syndrome

    Dichotomic 0/1, outcome defined from radiology reports.

    Measured: During the study period 1.1.2010-31.12.2020 wiht recorded sodium values.

Secondary outcomes (2)
  1. Epidemiology and correction rates of hyponatremia

    The prevalence of severe, and moderate hyponatremia in Tyks. The medium and maximal correction rate during any 24-hour period during the treatment period.

    Measured: During any 24-hour period during the treatment period.

  2. Prognosis linked to severe or moderate hyponatremia

    To assess 1, 6 and 12 month mortality and hospitalization duration compared to normal sodium values at enrollment.

    Measured: 1, 6 and 12 months after enrollment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Feb 2026
  2. Study start1 Sep 2023
  3. Primary completion1 Jan 2026
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Retrospective
Enrolment
10,000 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07430787
Sponsor's protocol ID
T194/2022-1
Status last verified
Feb 2026
First submitted
17 Feb 2026
Last updated
24 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Current Finnish legislation does not permit the sharing of individual participant data (IPD).

Publications

  • Kalampokini S, Artemiadis A, Zis P, Hadjihannas L, Parpas G, Kyrri A, Hadjigeorgiou GM. Osmotic demyelination syndrome improving after immune-modulating treatment: Case report and literature review. Clin Neurol Neurosurg. 2021 Sep;208:106811. doi: 10.1016/j.clineuro.2021.106811. Epub 2021 Jul 24.

    PubMed 34358802
  • Baek SH, Jo YH, Ahn S, Medina-Liabres K, Oh YK, Lee JB, Kim S. Risk of Overcorrection in Rapid Intermittent Bolus vs Slow Continuous Infusion Therapies of Hypertonic Saline for Patients With Symptomatic Hyponatremia: The SALSA Randomized Clinical Trial. JAMA Intern Med. 2021 Jan 1;181(1):81-92. doi: 10.1001/jamainternmed.2020.5519.

    PubMed 33104189
  • Verbalis JG, Goldsmith SR, Greenberg A, Schrier RW, Sterns RH. Hyponatremia treatment guidelines 2007: expert panel recommendations. Am J Med. 2007 Nov;120(11 Suppl 1):S1-21. doi: 10.1016/j.amjmed.2007.09.001.

    PubMed 17981159
  • Verbalis JG, Goldsmith SR, Greenberg A, Korzelius C, Schrier RW, Sterns RH, Thompson CJ. Diagnosis, evaluation, and treatment of hyponatremia: expert panel recommendations. Am J Med. 2013 Oct;126(10 Suppl 1):S1-42. doi: 10.1016/j.amjmed.2013.07.006.

    PubMed 24074529
  • Lambeck J, Hieber M, Dressing A, Niesen WD. Central Pontine Myelinosis and Osmotic Demyelination Syndrome. Dtsch Arztebl Int. 2019 Sep 2;116(35-36):600-606. doi: 10.3238/arztebl.2019.0600.

    PubMed 31587708

Questions about this trial

What is this clinical trial studying?

An observational study of Hyponatremia and Osmotic Demyelination Syndrome, run by University of Turku at 1 site in Finland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 24 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of ODS in hyponatremia patients (time frame: From enrollment to the end of the treamtent period. Usually 2-21 days.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07430787, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Feb 2026.

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