ClinicalTrials.Veeva

Menu

Cold Milk for Dysphagia in Preterm Infants

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Dysphagia of Newborn

Treatments

Other: Cold temperature (CS, at 4-9°C) of milk/formula
Other: Standard room temperature (RTS) feeding of milk/formula

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04421482
20-00876
R21HD100653 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

It is estimated that 30-70% of very low birth weight (VLBW) preterm infants will be diagnosed with swallowing dysfunction (dysphagia), which often leads to airway compromise in the form of laryngeal penetration and/or tracheal aspiration during oral feeding attempts. Chronic airway compromise results in a persistent inflammatory state, with disease progression that can be devastating for already fragile and developmentally immature lungs in preterm infants. At this time, there are limited therapeutic options for dysphagia in VLBW infants during oral feeding. In a recent publication, our research group was the first to demonstrate that short-duration of oral feeding with cold liquid reduces dysphagia occurrence from 71% to 26%. However, these data must be further validated for the effectiveness and safety of a full duration feeding before being recommended for routine clinical practice.

The objective is to identify preliminary evidence for the efficacy and safety of feeding full oral cold milk for dysphagia management in preterm infants. We hypothesize that oral feeding of cold milk in VLBW preterm infants with dysphagia will improve suck/swallow/breathe coordination and decrease penetration/ aspiration to the airway. We further hypothesize that cold milk intervention will have no adverse effects on intestinal blood flow, as assessed by Doppler Ultrasound. This is significant because there is a critical need to identify effective and safe evidence-based treatment options for dysphagia management in preterm infants.

This prospective study will seek to enroll Subjects who meet the following inclusion criteria: 1) VLBW (birth weight less than 1,500g and less than 32 weeks gestation), 2) admitted to NYU-Winthrop NICU, 3) Post-menstrual age (PMA) > 35 weeks at the time of the study, 4) receiving no or minimum respiratory support (<1 lit/min low-flow nasal cannula), 5) tolerating at least 50% of their enteral feeding orally, 6) having symptoms of swallowing dysfunction during oral feeding (clinical dysphagia) and 7) referred by the medical team for video fluoroscopic swallow study (VFSS) and/or fiberoptic endoscopic evaluation of swallowing (FEES).

To assess the efficacy of cold milk in treating dysphagia, study subjects will first have an oral motor feeding assessment using an FDA approved device called the nFant® Feeding Solution as well as VFSS and/or FEES. To assess the safety of using cold milk, subjects will receive a doppler ultrasound before and after the ingestion of cold liquid feeding to assess the mesenteric blood flow.

Enrollment

22 patients

Sex

All

Ages

35+ weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. VLBW (birth weight less than 1,500g and less than 32 weeks gestation)
  2. admitted to NYU-Winthrop NICU
  3. PMA > 35 weeks at the time of the study
  4. receiving no or minimum respiratory support (<1 lit/min low-flow nasal cannula)
  5. tolerating at least 50% of their enteral feeding orally and
  6. having symptoms of swallowing dysfunction during oral feeding (clinical dysphagia).
  7. referred by the medical team for VFSS and/or FEES assessments.

Exclusion criteria

Infants with other comorbidities, such as IUGR, upper airway anomalies, brain injury, neuromuscular disease, or life-threatening congenital disease.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

22 participants in 1 patient group

Very Low Birth Weight Preterm Infants
Other group
Description:
Very Low Birth Weight Preterm Infants (birth weight less than 1,500g and less than 32 weeks gestation) admitted to NYU Winthrop NICU. (n=42)
Treatment:
Other: Standard room temperature (RTS) feeding of milk/formula
Other: Cold temperature (CS, at 4-9°C) of milk/formula

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Nazeeh Hanna, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems