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Protein Supplementation in Hyponatremia Due to the Syndrome of Inappropriate Antidiuresis (TREASUREx)

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University Hospital Basel

Status

Enrolling

Conditions

Syndrome of Inappropriate Antidiuresis
Hyponatremia

Treatments

Dietary Supplement: Moltein PURE Protein Powder
Behavioral: Fluid restriction

Study type

Interventional

Funder types

Other

Identifiers

NCT06821802
2024-02282 kt25ChristCrain2;

Details and patient eligibility

About

The goal of this study is to assess the impact of protein supplementation on hyponatremia caused by the syndrome of inappropriate antidiuresis during hospitalization.

Full description

Hyponatremia (plasma sodium <135 mmol/L) is the most common electrolyte disorder, affecting up to 30% of hospitalized patients. Chronic hyponatremia (>48 hours) is linked to longer hospital stays, higher costs, increased mortality, and morbidity (e.g., falls, fractures, cognitive deficits). The most common cause of euvolemic hyponatremia is syndrome of inappropriate antidiuresis (SIAD), characterized by excessive water retention due to dysregulated vasopressin activity. Treatment options include fluid restriction or increasing water excretion with AVP antagonists, SGLT2 inhibitors, or oral urea.

A recent trial showed that protein supplementation can induce osmotic diuresis and raise sodium levels similarly to oral urea, with better tolerability. Since protein supplementation is often used in hospitalized patients with malnutrition, this study aims to compare its acceptability to fluid restriction in hospitalized SIAD patients. This head-to-head superiority trial will randomize patients to receive either 80 g of dietary protein daily or fluid restriction (1000 mL/day) for up to 5 days. The hypothesis is that protein supplementation is significantly more acceptable to patients than fluid restriction, ultimately improving treatment outcomes.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients with confirmed SIAD during the hospital stay or at screening, defined by:
  • Plasma sodium concentration <135 mmol/L
  • Plasma osmolality <300 mOsm/kg
  • Urine osmolality >100 mOsm/kg
  • Urine sodium concentration >30 mmol/L
  • Clinical euvolemia (no signs of hypovolemia or hypervolemia)

Exclusion criteria

  • Lactose intolerance, milk protein allergy, soy allergy, nuts allergy, or hypersensitivity to components of the protein supplement.
  • Inborn metabolic disorders affecting carbohydrate, lipid, or protein metabolism.
  • Severe symptomatic hyponatremia requiring 3% NaCl or intensive care.
  • New (within the last five days) treatment with SGLT2 inhibitors, vaptans or oral urea
  • Uncontrolled severe hypothyroidism (untreated)
  • Uncontrolled adrenal insufficiency (morning cortisol <150nmol/l)
  • eGFR <45 mL/min/1.73 m² (KDIGO G3b-5) or end-stage renal disease (dialysis)
  • Severe hepatic impairment or advanced symptomatic liver disease defined as past or current hepatic encephalopathy, liver cirrhosis Child C, or decompensated (bleeding, jaundice, hepatorenal syndrome)
  • Pregnancy, breastfeeding, or plans to become pregnant during the study.
  • End-of-life care
  • Lack of capacity or other reasons preventing from giving informed consent or following study procedures (e.g., due to language problems, psychological disorders, dementia, etc.)
  • Treatment with thiazid diuretic (must be stopped at least 48 hours before inclusion)

Post-randomization Exclusion Criteria:

  • Type 1 diabetes or uncontrolled type 2 diabetes (HbA1c >8.0%)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Protein Supplementation
Experimental group
Description:
80 g protein supplementation per day (two bottles, each containing 40 g protein)
Treatment:
Dietary Supplement: Moltein PURE Protein Powder
Fluid restriction
Active Comparator group
Description:
total daily fluid intake to a maximum of 1000 ml
Treatment:
Behavioral: Fluid restriction

Trial contacts and locations

1

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Central trial contact

Cemile Bathelt; Mirjam Christ-Crain, Prof. MD

Data sourced from clinicaltrials.gov

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