Use Of Nfant(R) Technology Feeding System For Infants Less Than 30 Weeks GA

Completed · Not applicable

Conditions studied: Prematurity, Extreme Prematurity

In brief

The purpose of the study is to utilize the objective data provided by the nfant® suite of products, along with current NICU visual assessment and cue-based feeding practices, in order to determine if feeding performance outcomes and clinical decision making for individualized feeding plans for premature infants born less than 30 weeks PMA are impacted.

Key facts

Study ID

NCT04256889

Run by

Woman's

People needed

23

Starts

2020-01-15

Expected to finish

2024-03-13

Last updated by the study team

2024-03-19

Who can join

Age: 0 and older, up to 1. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Infants less than or equal to 29 6/7 weeks gestation at birth

You may not qualify if…

• Infants 30 weeks or greater gestation at birth
• Infants with known or suspected congenital anomalies or chromosomal abnormalities
• Infants with diagnoses known to interfere with oral feeding, including, but not limited to cleft lip. cleft palate, gastroschisis, Tracheoesophageal fistula, micrognathia.
• History of Intraventricular hemorrhage Grade 3 or 4 or Periventricular Leukomalacia
• Infants with known diagnoses known to interfere with Gastrointestinal absorption, including, but not limited to, Necrotizing Enterocolitis requiring surgical intervention

Where it is running

• Woman's Hospital — Baton Rouge, Louisiana, United States

Full record on ClinicalTrials.gov

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