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Sodium Awareness in Lactation Trial

Sodium Awareness in Lactation Trial

Recruiting
Female
Phase N/A

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Overview

SALT is a multi-centre, non-blinded, non-randomized prospective interventional pilot study teaching lactating parents of hospitalized preterm infants how to test their breastmilk sodium (Na) using point-of-care (POC) meters. A drop in Na is a sign of secretory activation in the breast that is associated with adequate short and long-term breast milk volumes in this vulnerable population.

Primary Objective: Establish feasibility, acceptance, and time cost of parent-led parent milk Na testing in the first 14 days postpartum

Secondary Objective: Further investigate relationships between pumping behaviours, lactation risk factors, daily milk Na and lactation outcomes

Exploratory Objective: Explore how POC Na data may be used to modify pumping behaviour and milk volumes

Eligibility

Inclusion Criteria:

  1. Consent provided
  2. Have delivered a preterm singleton or twin infant at <35 weeks gestation admitted to a study NICU at birth or transferred into a study NICU from another NICU within the first 72 hours postpartum
  3. Day 5 or less postpartum (Day 1 = day of delivery) upon enrollment (ideally day 3 or less)
  4. Plans to lactate at least 2 weeks and initiate lactation with a breast pump
  5. Expected infant NICU stay of 7+ (ideally 14+) days in enrollment NICU(s)

Exclusion Criteria:

  1. Potential study participant's infant is critically ill and not expected to survive or has lethal diagnosis with plans by medical team/family to redirect care
  2. Has delivered triplets or higher order multiples (potential confounder for lactation challenges; of note, triplets or higher are rare, on the order of a few parents annually)
  3. Lactation contraindication(s) (i.e., active chemotherapy) or declines lactation initiation
  4. History of breast surgery that may affect ability to lactate (i.e., breast reduction; breast augmentation that utilized nipple incisions)
  5. Using or planning to use hormonal birth control in the first 14 days post-partum as may affect secretory activation/lactation
  6. Unable/unwilling to be present in study NICU during any of first 5 days postpartum
  7. Presumption by the medical team that infant will be in study NICU for <5 days

Study details
    Breastfeeding
    Preterm Birth
    Breast Pumping
    Lactation; Insufficient
    Partial

NCT06563726

The Hospital for Sick Children

15 October 2025

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