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Efficacy and Safety of Rapid Intermittent Compared With Slow Continuous Correction in Severe Hyponatremia Patients

Primary Purpose

Hyponatremia Symptomatic

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
3% hypertonic saline
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyponatremia Symptomatic focused on measuring Hyponatremia, Hypertonic saline, Treatment, Osmotic demyelination syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • In emergency setting (2016.6-) and/or inpatients at ward (2018.9-)
  • Glucose corrected serum sodium ≤125 mmol/L
  • Patients with moderately severe or severe symptom

    • Moderately severe

      :Nausea without vomiting Drowsy, Headache General weakness, myalgia

    • Severe :Vomiting, Stupor, Seizures, Coma (Glasgow Coma Scale ≤8)
  • written consent

Exclusion Criteria:

  • Pseudohyponatremia: serum osmolality > 275 mOsm/kg

    - If the serum osmolality is > 275 mOsm/kg but the BUN is ≥ 30 mg/dL, the patients can be registered if calculated serum osmolality (2 x plasma [Na] + [Glucose]/18) is <275 mOsm/kg

  • Primary polydipsia: urine osmolality ≤ 100 mOsm/kg
  • Glucose corrected serum sodium >125 mmol/L
  • Arterial hypotension (SBP <90mmHg and MAP <70mmHg)
  • Anuria or urinary outlet obstruction
  • Liver disease

    • transaminase levels >3 times the upper limit normal
    • Known LC with ascites or diuretics use or PSE Hx or Varix Hx
  • Uncontrolled diabetes mellitus (HbA1C > 9%)
  • Women who are pregnant or breast feeding
  • History of cardiac surgery excluding PCA, acute myocardial infarction, sustained ventricular tachycardia, ventricular fibrillation, acute coronary syndrome, cebrovascular trauma, and increased intracranial pressure within the 3 months prior to randomization

Sites / Locations

  • Hallym University Dongtan Sacred Hospital
  • Seoul National University Bundang Hospital Clinical Trial Center
  • Seoul National University Boramae Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Intermittent bolus group

slow continuous infusion group

Arm Description

<<Within 6hr>> Moderately Severe : 3% saline 2ml/kg over 20min *1 (unknown bwt 100ml) Severe :3% saline 2ml/kg over 20min *2 (unknown bwt 100ml) <additional treatment> Repeat 3% saline 2ml/kg over 20min at every sample time point (at 1/6hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 6-24hr>> - Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point(at 12/18/24hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 24-48hr>> Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point (at 30/36/42/48hr) till Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief

<<Within 24hr>> - Moderately Severe: 3% saline 0.5ml/kg/hr (unknown bwt 25ml/hr) - Severe: 3% saline 1ml/kg/hr (unknown bwt 50ml/hr) Infusion protocol modification as below by Na at every sample time point (at 1/6/12/18/24 hr) If Na 5-9 mmol/L inc from initial Na and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <0.5mmol/hr or △ Na inc <3mmol/6hr : add 0.25ml/kg/hr, restart 0.5ml/kg/hr if previously stopped if △ Na inc ≥0.5mmol/hr or △ Na inc ≥ 3mmol/6hr : maintain infusion rate <<During 24-48hr>> - Moderately Severe and Severe Infusion protocol modification as below by Na at every sample time point (at 30/36/42/48hr) If Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <1.5mmol/6hr : add 0.25ml/kg/hr or restart 0.25ml/kg/hr if previously stopped if △ Na inc ≥ 1.5mmol/6hr : maintain infusion rate

Outcomes

Primary Outcome Measures

Incidence of overcorrection rate at any given period
Increase in sNa by >12 mmol/L within 24 hours or Increase in sNa by >18 mmol/L within 48 hours All subjects receive hypertonic saline by intermittent bolus or slow continuous infusion for 48 hours, serum Na will be measured.

Secondary Outcome Measures

Rapid improvement of symptoms
Change of symptoms from baseline to 24 hours after hypertonic fluid treatment
Time from treatment initiation to an increase of serum Na ≥ 5 mmol/L
Incidence of target correction rate
Target correction rate is defined by achieved serum Na <10 mmol/L within 24 hours, achieved serum Na <18 mmol/L within 48 hours
Time to serum Na >130 mmol/L
Time from treatment initiation to achieved serum Na> 130mmol/L
Length of hospital stay
Incidence of additional treatment
Additional treatment is performed if symptom is not relieved or undercorrection develops (achieved Na < 5mmol/L with 24 hours or achieved Na <12mmol/L within 48 hours)
Incidence of osmotic demyelinating syndrome confirmed by ICD -10 code or MRI
Incidence of relowering treatment
Relowering treatment is performed as below if achieved serum Na is <10 mmol/L within 24 hours, achieved serum Na is <18 mmol/L within 48 hours. discontinuing ongoing active treatment start infusion of 10ml/kg of 5% dextrose over 1hr ± desmopressin 2mcg IV
Change of Glasgow coma scale (GCS) ≤8
Change in GCS of hyponatremia symptoms at pretreatment, 24 hours, and 48 hours after treatment

Full Information

First Posted
August 1, 2016
Last Updated
April 7, 2020
Sponsor
Seoul National University Hospital
Collaborators
National Research Foundation of Korea
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1. Study Identification

Unique Protocol Identification Number
NCT02887469
Brief Title
Efficacy and Safety of Rapid Intermittent Compared With Slow Continuous Correction in Severe Hyponatremia Patients
Official Title
Efficacy and Safety of Rapid Intermittent Correction Compared With Slow Continuous Correction With Hypertonic Saline in Patient With Moderately Severe or Severe Symptomatic Severe Hyponatremia (SALSA Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
August 2016 (undefined)
Primary Completion Date
September 30, 2019 (Actual)
Study Completion Date
September 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
Collaborators
National Research Foundation of Korea

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will investigate efficacy and safety of rapid intermittent correction compared with slow continuous correction with hypertonic saline in patient with moderately severe or severe symptomatic severe hyponatremia
Detailed Description
Moderate to severe symptomatic hyponatremia requires prompt treatment with hypertonic saline. The extent and rate of increase in serum sodium (sNa) levels during treatment are critical. Several methods for continuous infusion of hypertonic saline were used to guide rate of fluid administered to achieve the required serum sodium target. As based on static model, they had a bias to over-correction of hyponatremia. Alternative approach to treatment with hypertonic fluid is to use small, fixed boluses to achieve controlled increments in sNa. However, there was no high quality evidence on whether hypertonic saline are best given in continuous infusion (preferred by most) or bolus injection. The aim of present study, a multi-center (Seoul National University Bundang Hospital [2016.8~], Seoul National University Boramae Medical Center [2016. 9~], Hallym University Dongtan Sacred Heart Hospital [2017.7~]), randomized, open labelled, controlled clinical trial, is to investigate efficacy and safety of rapid intermittent correction compared with slow continuous correction with hypertonic saline in patient with moderately severe or severe symptomatic severe hyponatremia. A total 178 patients, who suffer from symptomatic severe hyponatremia, will be enrolled and randomly assigned to receive either intermittent bolus infusion or slow continuous infusion by 3% hypertonic saline. Subjects will take different rate of 3% hypertonic saline for 24-48 hours stratified by severity of clinical symptoms. Serum sodium will be measured at every six hours during two days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyponatremia Symptomatic
Keywords
Hyponatremia, Hypertonic saline, Treatment, Osmotic demyelination syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
178 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intermittent bolus group
Arm Type
Active Comparator
Arm Description
<<Within 6hr>> Moderately Severe : 3% saline 2ml/kg over 20min *1 (unknown bwt 100ml) Severe :3% saline 2ml/kg over 20min *2 (unknown bwt 100ml) <additional treatment> Repeat 3% saline 2ml/kg over 20min at every sample time point (at 1/6hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 6-24hr>> - Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point(at 12/18/24hr) till Na 5-9 mmol/L inc from initial Na and sx relief <<During 24-48hr>> Moderately Severe or Severe : Repeat 3% saline 2ml/kg over 20min at every sample time point (at 30/36/42/48hr) till Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief
Arm Title
slow continuous infusion group
Arm Type
Active Comparator
Arm Description
<<Within 24hr>> - Moderately Severe: 3% saline 0.5ml/kg/hr (unknown bwt 25ml/hr) - Severe: 3% saline 1ml/kg/hr (unknown bwt 50ml/hr) Infusion protocol modification as below by Na at every sample time point (at 1/6/12/18/24 hr) If Na 5-9 mmol/L inc from initial Na and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <0.5mmol/hr or △ Na inc <3mmol/6hr : add 0.25ml/kg/hr, restart 0.5ml/kg/hr if previously stopped if △ Na inc ≥0.5mmol/hr or △ Na inc ≥ 3mmol/6hr : maintain infusion rate <<During 24-48hr>> - Moderately Severe and Severe Infusion protocol modification as below by Na at every sample time point (at 30/36/42/48hr) If Na 10-17 mmol/L inc from initial Na or Na ≥ 130mmol and sx relief : stop 3% saline infusion regardless of △ Na if △ Na inc <1.5mmol/6hr : add 0.25ml/kg/hr or restart 0.25ml/kg/hr if previously stopped if △ Na inc ≥ 1.5mmol/6hr : maintain infusion rate
Intervention Type
Drug
Intervention Name(s)
3% hypertonic saline
Intervention Description
The same as above
Primary Outcome Measure Information:
Title
Incidence of overcorrection rate at any given period
Description
Increase in sNa by >12 mmol/L within 24 hours or Increase in sNa by >18 mmol/L within 48 hours All subjects receive hypertonic saline by intermittent bolus or slow continuous infusion for 48 hours, serum Na will be measured.
Time Frame
up to 48 hours
Secondary Outcome Measure Information:
Title
Rapid improvement of symptoms
Description
Change of symptoms from baseline to 24 hours after hypertonic fluid treatment
Time Frame
up to 24 hours
Title
Time from treatment initiation to an increase of serum Na ≥ 5 mmol/L
Time Frame
up to 48 hours
Title
Incidence of target correction rate
Description
Target correction rate is defined by achieved serum Na <10 mmol/L within 24 hours, achieved serum Na <18 mmol/L within 48 hours
Time Frame
up to 48 hours
Title
Time to serum Na >130 mmol/L
Description
Time from treatment initiation to achieved serum Na> 130mmol/L
Time Frame
up to 48 hours
Title
Length of hospital stay
Time Frame
up to 8 weeks
Title
Incidence of additional treatment
Description
Additional treatment is performed if symptom is not relieved or undercorrection develops (achieved Na < 5mmol/L with 24 hours or achieved Na <12mmol/L within 48 hours)
Time Frame
up to 48 hours
Title
Incidence of osmotic demyelinating syndrome confirmed by ICD -10 code or MRI
Time Frame
up to 48 hours
Title
Incidence of relowering treatment
Description
Relowering treatment is performed as below if achieved serum Na is <10 mmol/L within 24 hours, achieved serum Na is <18 mmol/L within 48 hours. discontinuing ongoing active treatment start infusion of 10ml/kg of 5% dextrose over 1hr ± desmopressin 2mcg IV
Time Frame
up to 48 hours
Title
Change of Glasgow coma scale (GCS) ≤8
Description
Change in GCS of hyponatremia symptoms at pretreatment, 24 hours, and 48 hours after treatment
Time Frame
up to 48 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: In emergency setting (2016.6-) and/or inpatients at ward (2018.9-) Glucose corrected serum sodium ≤125 mmol/L Patients with moderately severe or severe symptom Moderately severe :Nausea without vomiting Drowsy, Headache General weakness, myalgia Severe :Vomiting, Stupor, Seizures, Coma (Glasgow Coma Scale ≤8) written consent Exclusion Criteria: Pseudohyponatremia: serum osmolality > 275 mOsm/kg - If the serum osmolality is > 275 mOsm/kg but the BUN is ≥ 30 mg/dL, the patients can be registered if calculated serum osmolality (2 x plasma [Na] + [Glucose]/18) is <275 mOsm/kg Primary polydipsia: urine osmolality ≤ 100 mOsm/kg Glucose corrected serum sodium >125 mmol/L Arterial hypotension (SBP <90mmHg and MAP <70mmHg) Anuria or urinary outlet obstruction Liver disease transaminase levels >3 times the upper limit normal Known LC with ascites or diuretics use or PSE Hx or Varix Hx Uncontrolled diabetes mellitus (HbA1C > 9%) Women who are pregnant or breast feeding History of cardiac surgery excluding PCA, acute myocardial infarction, sustained ventricular tachycardia, ventricular fibrillation, acute coronary syndrome, cebrovascular trauma, and increased intracranial pressure within the 3 months prior to randomization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seon Ha Baek, PhD
Organizational Affiliation
Hallym University Dongtan Sacred Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hallym University Dongtan Sacred Hospital
City
Hwaseong-si
State/Province
Gyeonggi-do
ZIP/Postal Code
445-907
Country
Korea, Republic of
Facility Name
Seoul National University Bundang Hospital Clinical Trial Center
City
Seongnam
State/Province
Gyeonggi-do
ZIP/Postal Code
13605
Country
Korea, Republic of
Facility Name
Seoul National University Boramae Hospital
City
Seoul
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24569125
Citation
Spasovski G, Vanholder R, Allolio B, Annane D, Ball S, Bichet D, Decaux G, Fenske W, Hoorn EJ, Ichai C, Joannidis M, Soupart A, Zietse R, Haller M, van der Veer S, Van Biesen W, Nagler E; Hyponatraemia Guideline Development Group. Clinical practice guideline on diagnosis and treatment of hyponatraemia. Eur J Endocrinol. 2014 Feb 25;170(3):G1-47. doi: 10.1530/EJE-13-1020. Print 2014 Mar. Erratum In: Eur J Endocrinol. 2014 Jul;171(1):X1.
Results Reference
result
PubMed Identifier
33104189
Citation
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.
Results Reference
derived
PubMed Identifier
28356136
Citation
Lee A, Jo YH, Kim K, Ahn S, Oh YK, Lee H, Shin J, Chin HJ, Na KY, Lee JB, Baek SH, Kim S. Efficacy and safety of rapid intermittent correction compared with slow continuous correction with hypertonic saline in patients with moderately severe or severe symptomatic hyponatremia: study protocol for a randomized controlled trial (SALSA trial). Trials. 2017 Mar 29;18(1):147. doi: 10.1186/s13063-017-1865-z.
Results Reference
derived

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Efficacy and Safety of Rapid Intermittent Compared With Slow Continuous Correction in Severe Hyponatremia Patients

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