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临床试验/NCT07562997
NCT07562997招募中不适用

Sodium and Milk Fortification Evaluation of Body Composition Among Very Preterm Infants

University of Washington3 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2026年5月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
150
试验地点
3
主要终点
Body composition by point-of-care ultrasound

研究概览

简要总结

The goal of the trial is to learn if targeted sodium supplementation (including blood and urine sodium testing) versus standard milk fortification (including blood sodium testing) improves growth and body composition in very preterm infants?

详细描述

Very preterm infants (born <32 weeks gestational age) are at high risk for postnatal growth faltering, which is associated with adverse neurodevelopmental outcomes. Despite routine use of enriched human milk fortification in the NICU, many infants fail to achieve adequate somatic and lean mass growth. Sodium depletion has been identified as a potentially modifiable contributor to this problem: renal tubular immaturity in preterm infants results in obligate urinary sodium wasting. Total body sodium depletion has been associated with poor growth in infants and poor muscle mass development in animal studies.

Current NICU practice relies primarily on serum sodium to guide supplementation; however, serum sodium is a late and insensitive marker of total body sodium depletion. Urine sodium is a more sensitive indicator of sodium balance and may identify depletion before serum levels fall. Gestational-age-specific urine sodium thresholds to guide supplementation have recently been proposed (Stalter et al., 2025), but have evaluated body composition in a prospective randomized trial.

This trial tests whether a structured, urine sodium-guided supplementation protocol based on every other week urine and serum sodium monitoring improves anthropometric growth and lean mass accrual compared to standard enriched fortification alone. The intervention runs from day of life 14 through 36 weeks postmenstrual age, with tapering through 38 weeks PMA.

Body composition assessment incorporates two complementary modalities: serial point-of-care ultrasound (POCUS) of the biceps, rectus femoris, and subcutaneous fat for longitudinal lean and fat mass tracking, and Air Displacement Plethysmography (PeaPod) at 36 weeks postmenstrual age or discharge for criterion-standard whole-body composition. Fat mass, fat-free mass, and body fat percentage will be referenced against the Norris et al. preterm normative curves.

The trial uses an open-label design with block randomization stratified by gestational age. A Data Safety and Monitoring Board will conduct oversight and interim safety reviews.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
0 Days 至 14 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Admitted to the University of Washington, Oregon Health and Sciences, or University of Cincinnati NICU at 14 days of age
  • Born between 24w0days and 31w6d
  • Achieved full enteral feeding

排除标准

  • Congenital or chromosomal anomalies affecting growth
  • Acute renal insufficiency (KDIGO stage 1 or higher)
  • Necrotizing enterocolitis (modified Bell's stage IIA or higher)
  • Anticipated NICU stay less than 30 days
  • Enrollment in a concurrent interventional study that may confound study outcomes

研究组 & 干预措施

Targeted sodium supplementation

Experimental

Every two weeks serum sodium and urine sodium testing with sodium supplementation if indicated by algorithm. Milk fortification per growth metrics.

干预措施: Serum sodium testing (Diagnostic Test)

Targeted sodium supplementation

Experimental

Every two weeks serum sodium and urine sodium testing with sodium supplementation if indicated by algorithm. Milk fortification per growth metrics.

干预措施: Milk fortification (Dietary Supplement)

Enriched Milk Fortification

Active Comparator

Serum sodium testing every two weeks with sodium supplementation if indicated by clinical team. Milk fortification per growth metrics.

干预措施: Serum sodium testing (Diagnostic Test)

Enriched Milk Fortification

Active Comparator

Serum sodium testing every two weeks with sodium supplementation if indicated by clinical team. Milk fortification per growth metrics.

干预措施: Milk fortification (Dietary Supplement)

Targeted sodium supplementation

Experimental

Every two weeks serum sodium and urine sodium testing with sodium supplementation if indicated by algorithm. Milk fortification per growth metrics.

干预措施: Urine sodium testing (Diagnostic Test)

结局指标

主要结局

Body composition by point-of-care ultrasound

时间窗: Enrollment to study completion, on average 4-10 weeks

Evaluate muscle and subcutaneous fat accretion from enrollment to 36 weeks posmtnestrual age. The study team will perform biceps and rectus femoris cross-sectional area measurements using point-of-care ultrasound every 2 weeks. We will perform arm and mid-thigh subcutaneous fat measurements using point-of-care ultrasound every 2 weeks.

次要结局

  • Body composition using air-displacement plethysmography(At study completion, on average 4-10 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Katie Strobel

Assistant Professor: Pediatrics

University of Washington

研究点 (3)

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