A Randomized Controlled Trial of Impact of Wearable, Wireless Breast Pumps on Frequency and Efficacy of Milk Expression in Mothers of Premature Infants (NCT06723067)

🧪 Interventions in This Study

• Wearable wireless breast pump (DEVICE)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• Ascension Seton Medical Center — Austin, Texas

📞 Contact the Study Coordinator

Phone: (512) 324-1085

Email: erica.ortiz@ascension.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

• 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
• Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
• Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Premature Birth

• Skin-to-skin After Delivery in Preterm Infants Born at 28-32 Weeks of Gestation — Halifax,
• Local Version of the Multi-center PREVENT Study Evaluating Cardio-respiratory Instability in Premature Infants — Chicago, Illinois
• NICU Antibiotics and Outcomes (NANO) Follow-up Study — San Diego, California
• Wireless MicroPremVitals Button Sensor in the NICU — Montreal, Quebec
• Growing Little PEAPODS Study — Madison, Wisconsin
• A Randomized Control Trial of a Responsive Parenting Intervention to Support Healthy Brain Development and Self-regulation in Toddlers Born Preterm — Houston, Texas

Explore by condition: All Premature Birth clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Contact the study coordinator using the phone/email above.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.