Actively Recruiting
Analysis of Factors Influencing Full Oral Feeding Acquisition in Very Preterm Infants
Led by Hospices Civils de Lyon · Updated on 2024-10-18
170
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating oral disorders in extremely premature infants born before 29 weeks, focusing on the age at which these infants achieve full oral feeding without the need for tube feeding. The study aims to understand the development of oral skills in this population, as oral disorders can lead to delayed feeding autonomy and longer hospital stays, impacting psychomotor and cognitive development. It also seeks to identify risk factors for delayed oral feeding and calculate the incidence of oral feeding disorders up to 24 months of age. The study monitors infants admitted to a neonatal unit where a daily tactile stimulation protocol of orality is applied by nurses and physiotherapists to support the development of oral skills. This protocol involves stroking cheeks and peri-oral and intra-oral areas to encourage oral feeding autonomy. The study is observational and focuses on infants born between 2018 and 2021 who received this care approach during their hospital stay. Participants will be followed from birth until they reach full oral feeding autonomy, with the main measurement being the corrected gestational age at this time, observed up to two months. Researchers will also analyze risk factors for delayed oral feeding and track oral feeding disorders over a longer term. Data collection includes monitoring feeding progress and hospital discharge details, with participant involvement ending when oral feeding autonomy is achieved or after 24 months for disorder incidence assessment.
CONDITIONS
Brief Title
Acquisition of Full Oral Feeding and Further Oral Disorders in Extremely Preterm Infants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infants born at a gestational age of 28 weeks or less
- Born between January 1, 2018 and December 31, 2021
- Admitted to the neonatology department within the first three days of life
- Discharged directly to home or to a nursery
You will not qualify if you...
- Infants transferred to another department during hospitalization
- Infants with severe pathology requiring surgical management in the first weeks of life (excluding inguinal hernia repair)
- Infants with severe malformations
- Parents refuse to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to two months
Participants who undergo routine care are observed to determine the age of acquisition of full oral feeding with specific and individualized stimulation of orality.
Trial Site Locations
Total: 1 location
1
Hopital Croix Rousse
Lyon, France
Actively Recruiting
Research Team
P
Pr PICAUD Jean-Charles, MD, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Frequently Asked Questions
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