Partnering With Parents for Pumping Success: Feasibility of Personalized Lactation Support Utilizing Point-of-Care Human Milk Biomarkers

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: Female
Healthy Volunteers: f
View:

• Consent provided

• 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

• Day 5 or less postpartum (Day 1 = day of delivery) upon enrollment (ideally day 3 or less)

• Plans to lactate at least 2 weeks and initiate lactation with a breast pump

• Expected infant NICU stay of 7+ (ideally 14+) days in enrollment NICU(s)

Locations
United States
Washington
Seattle Children's Hospital
RECRUITING
Seattle
University of Washington Medical Center - Montlake
RECRUITING
Seattle
Contact Information
Primary
Samantha J. Anthony, PhD
samantha.anthony@sickkids.ca
(416) 813-7654
Backup
Rebecca Hobban, MD, MPH
Rebecca.Hoban@seattlechildrens.org
Time Frame
Start Date: 2025-03-10
Estimated Completion Date: 2026-03
Participants
Target number of participants: 40
Related Therapeutic Areas
Sponsors
Leads: The Hospital for Sick Children
Collaborators: University of Washington

This content was sourced from clinicaltrials.gov

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