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Physiologic Approach to Sodium Supplementation in Premature Infants (Salt to Grow)

Primary Purpose

Postnatal Growth Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Sodium supplementation guided by urine sodium concentration algorithm
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postnatal Growth Disorder focused on measuring Postnatal Growth Disorder, Growth and development

Eligibility Criteria

7 Days - 16 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Infants with gestational age 25 0/7 - 29 6/7 at birth
  2. Birth weight ≥ 500 grams
  3. Admitted within the 1st week of life
  4. < 17 days of age at time of enrollment

Exclusion Criteria:

  1. Infants admitted after the 1st week of life
  2. Major congenital anomalies
  3. Structural genitourinary abnormality
  4. Renal dysfunction (serum creatinine > 1.0 mg/dl or an increase of ≥ 0.3 mg/dl between the 2 most recent consecutive measurements) immediately prior to the initiation of study procedures.
  5. Diuretic use less than 48 hours prior to initiation of study procedures
  6. Infant with an ostomy (infants receiving an ostomy after study entry will be withdrawn)
  7. Infant with a diagnosis or suspicion of diabetes insipidus

Sites / Locations

  • Indiana University Health North
  • Riley Hospital for Children at IU Health
  • Sidney and Lois Eskenazi Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control

Sodium supplementation algorithm

Arm Description

Standard of care sodium supplementation as directed by the medical care team

Beginning on the 14th -16th postnatal day and continuing until 36 weeks postmenstrual age, infants randomized to the algorithm will have a spot urine sodium concentration determined every two weeks and sodium supplementation provided according to the algorithm.

Outcomes

Primary Outcome Measures

Change in somatic growth (weight)
evaluated by the change in Z-score
Change in somatic growth (length)
evaluated by the change in Z-score
Change in somatic growth (head circumference)
evaluated by the change in Z-score

Secondary Outcome Measures

Change in somatic growth (weight)
evaluated by the change in Z-score
Change in somatic growth (length)
evaluated by the change in Z-score
Change in somatic growth (head circumference)
evaluated by the change in Z-score
Total body water
Measured by the doubly labeled water method
Energy expenditure
Measured by the doubly labeled water method
Incidence and severity of bronchopulmonary dysplasia (BPD)
as defined by the 2000 NICHD Workshop on BPD
Duration of mechanical ventilation
days on assisted ventilation
Need for supplemental oxygen
days on oxygen supplementation
Use of diuretic therapy
frequency of use
Retinopathy of prematurity
worst grade

Full Information

First Posted
March 18, 2019
Last Updated
September 28, 2023
Sponsor
Indiana University
Collaborators
Thrasher Research Fund
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1. Study Identification

Unique Protocol Identification Number
NCT03889197
Brief Title
Physiologic Approach to Sodium Supplementation in Premature Infants
Acronym
Salt to Grow
Official Title
Physiologic Approach to Sodium Supplementation in Premature Infants
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
July 22, 2023 (Actual)
Study Completion Date
August 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indiana University
Collaborators
Thrasher Research Fund

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Postnatal growth failure occurs in up to 50% of very low birth weight (VLBW, <1500 grams at birth) infants as assessed by discharge weight. This study will evaluate if a sodium supplementation algorithm guided by spot urine sodium measurements can improve postnatal growth.
Detailed Description
Postnatal growth failure is a significant morbidity in very low birth weight (VLBW, <1500 grams at birth) infants. Efforts to promote growth and optimize nutritional support have included earlier initiation of parenteral nutrition and increased caloric and protein administration. While these advances in nutritional practices have resulted in improved growth, up to 50% of VLBW infants continue to experience postnatal growth failure (defined as discharge weight <10th percentile by Fenton growth charts) and over 25% experience severe postnatal growth failure (<3rd percentile). Current nutritional recommendations for sodium provision to preterm infants is 3-5 mEq/kg/d and fails to take into account the degree of renal immaturity present in extremely preterm infants. The investigators hypothesize that the sodium supplementation algorithm will improve in-hospital somatic growth (weight, length, and head circumference) between 2 weeks of postnatal age and 36 weeks postmenstrual age over current sodium replacement practices. The algorithm will be evaluated in a prospective, pragmatic, randomized trial. Infants in the sodium supplementation algorithm group will have a spot urine sodium concentration determined every two weeks beginning on the 14th postnatal day and continuing until 36 weeks postmenstrual age with sodium supplementation provided according to the algorithm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postnatal Growth Disorder
Keywords
Postnatal Growth Disorder, Growth and development

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Data entered as group A and B.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard of care sodium supplementation as directed by the medical care team
Arm Title
Sodium supplementation algorithm
Arm Type
Active Comparator
Arm Description
Beginning on the 14th -16th postnatal day and continuing until 36 weeks postmenstrual age, infants randomized to the algorithm will have a spot urine sodium concentration determined every two weeks and sodium supplementation provided according to the algorithm.
Intervention Type
Drug
Intervention Name(s)
Sodium supplementation guided by urine sodium concentration algorithm
Intervention Description
4 mEq/kg/d sodium added the first time urine [Na] below threshold; for each subsequent time urine [Na] below threshold, add additional 2 mEq/kg/d.
Primary Outcome Measure Information:
Title
Change in somatic growth (weight)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and 36 weeks conceptual age
Title
Change in somatic growth (length)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and 36 weeks conceptual age
Title
Change in somatic growth (head circumference)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and 36 weeks conceptual age
Secondary Outcome Measure Information:
Title
Change in somatic growth (weight)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and discharge or transfer from the NICU or 44 weeks corrected age (whichever occurs first)
Title
Change in somatic growth (length)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and discharge or transfer from the NICU or 44 weeks corrected age (whichever occurs first)
Title
Change in somatic growth (head circumference)
Description
evaluated by the change in Z-score
Time Frame
between 2 weeks of age and discharge or transfer from the NICU or 44 weeks corrected age (whichever occurs first)
Title
Total body water
Description
Measured by the doubly labeled water method
Time Frame
32 weeks conceptual age
Title
Energy expenditure
Description
Measured by the doubly labeled water method
Time Frame
32 weeks conceptual age
Title
Incidence and severity of bronchopulmonary dysplasia (BPD)
Description
as defined by the 2000 NICHD Workshop on BPD
Time Frame
36 weeks conceptual age
Title
Duration of mechanical ventilation
Description
days on assisted ventilation
Time Frame
36 weeks conceptual age
Title
Need for supplemental oxygen
Description
days on oxygen supplementation
Time Frame
36 weeks conceptual age
Title
Use of diuretic therapy
Description
frequency of use
Time Frame
36 weeks conceptual age
Title
Retinopathy of prematurity
Description
worst grade
Time Frame
36 weeks conceptual age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Days
Maximum Age & Unit of Time
16 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants with gestational age 25 0/7 - 29 6/7 at birth Birth weight ≥ 500 grams Admitted within the 1st week of life < 17 days of age at time of enrollment Exclusion Criteria: Infants admitted after the 1st week of life Major congenital anomalies Structural genitourinary abnormality Renal dysfunction (serum creatinine > 1.0 mg/dl or an increase of ≥ 0.3 mg/dl between the 2 most recent consecutive measurements) immediately prior to the initiation of study procedures. Diuretic use less than 48 hours prior to initiation of study procedures Infant with an ostomy (infants receiving an ostomy after study entry will be withdrawn) Infant with a diagnosis or suspicion of diabetes insipidus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gregory M Sokol, MD
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jeffrey L Segar, MD
Organizational Affiliation
Medical College Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University Health North
City
Carmel
State/Province
Indiana
ZIP/Postal Code
46032
Country
United States
Facility Name
Riley Hospital for Children at IU Health
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
Sidney and Lois Eskenazi Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29486497
Citation
Segar DE, Segar EK, Harshman LA, Dagle JM, Carlson SJ, Segar JL. Physiological Approach to Sodium Supplementation in Preterm Infants. Am J Perinatol. 2018 Aug;35(10):994-1000. doi: 10.1055/s-0038-1632366. Epub 2018 Feb 27.
Results Reference
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Physiologic Approach to Sodium Supplementation in Premature Infants

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