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

NCT04256889 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2024-03-19

No results posted yet for this study

Summary

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.

Conditions

  • Prematurity
  • Extreme Prematurity

Interventions

DEVICE

nfant(R) feeding system

Use of nfant(R) technology feeding system as an adjunct to visual assessment and cue-based feedings for infants born less than 30 weeks GA

Sponsors & Collaborators

  • NFANT Labs

    collaborator UNKNOWN

  • Woman's

    lead OTHER

Principal Investigators

  • Nanette Gremillion, PT, MS, CNT · Woman's Hospital, Louisiana

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Weeks
Max Age
29 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-15
Primary Completion
2024-03-13
Completion
2024-03-13
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04256889 on ClinicalTrials.gov