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NCT07219784

Abdominal Binders to Minimize Enteral Nutrition Disruptions for Preterm Infants On Non-Invasive Respiratory Support

Enrolling by Invitation
NAUp to 1InterventionalTreatment
Albany Medical College
~120 participants
Updated 2025-10-22 on ClinicalTrials.gov
What's tested:An abdominal binder

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Days with interruptions to the feeding protocol
Measured over During initial hospitalization in the NICU after infant is enrolled in the study (assessed up to 6 months).

Conditions

Feeding Intolerance
Abdominal Distension

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NCT07219784

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Albany Med Health System

    Albany, New Yorkno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Anshu Paul, MD · PRINCIPAL_INVESTIGATOR · Albany Med Health System

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Born at \<32w0d GA
Chronologic age \>7 days, treatment or control protocol started by 21 days of life
On non-invasive positive pressure respiratory support (NIMV or CPAP), either as primary support or after extubation from invasive mechanical ventilation
Has received 80 mL/kg/day of feeds at least once

Exclusion

Skin integrity concerns
Known abdominal or respiratory anomalies
Umbilical lines in place
Transferred to AMC NICU after 7 days of life
Known genetic or major anatomic anomalies

What this trial measures

  • Days with interruptions to the feeding protocolDuring initial hospitalization in the NICU after infant is enrolled in the study (assessed up to 6 months).

    Days with interruptions to the feeding protocol, defined as interruptions to feeds or advances per our unit protocol for the infant's GA and birth weight (BW), due to feeding intolerance, defined as abdominal distension, increase in abdominal girth, abnormal stooling pattern, abdominal tenderness, increase in gastric residuals, emesis, and feeding-related cardiorespiratory events.