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The Multi-disciplinary Approach of Children With Feeding Difficulties and Tube Feeding in UZB Between 2000 and 2021 (ORALAV)

U

Universitair Ziekenhuis Brussel

Status

Invitation-only

Conditions

Enteral Nutrition
Parenteral Nutrition
Tube Feeding
Oral Aversion

Treatments

Combination Product: Structured multi-disciplinary approach

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this Retrospective Cohort Study is to compare the patients from before and after the implementation of the pre-convention for infants with feeding difficulties needing tube feeding or having received tube feeding in the past, but able to develop normal feeding behavior.

The main objectives it aims to compare are:

  • To characterize the patients taking part in a multi-disciplinary follow-up for feeding difficulties over time and to evaluate their progress before and after the institution of a multidisciplinary team in the context of the pre-convention for feeding difficulties from the RIZIV/INAMI.
  • To evaluate if the multi-disciplinary approach is more efficient for treatment and follow-up in infants with eating difficulties before and after the start of the pre-convention.
  • To calculate the probability of reaching full oral intake after having feeding difficulties within two years.

Enrollment

330 estimated patients

Sex

All

Ages

Under 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2000 and the 31st of December 2021 and receiving the label "feeding difficulties".

The infants have a pediatric feeding disorder that prevent them from feeding normally by oral means.

  • The infants need or have needed (enteral or parenteral) artificial nutrition.
  • The infants are aged between 0 and 12 years at their first presentation.
  • The infants are capable of developing normal feeding behavior.

Exclusion criteria

  • Have no 6-months follow-up available.
  • Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.

Trial design

330 participants in 2 patient groups

Group 1
Description:
Infants who consulted between January 1st 2000 and December 31st 2009 (this is before the implementation of the pre-convention). Inclusion criteria: * Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2000 and the 31st of December 2009 and receiving the label "feeding difficulties". * The infants have a pediatric feeding disorder that prevent them from feeding normally by oral means. * The infants need or have needed (enteral or parenteral) artificial nutrition. * The infants are aged between 0 and 12 years at their first presentation. * The infants are capable of developing normal feeding behavior. Infants will be excluded from this study if they: * Have no 6-months follow-up available. * Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.
Group 2
Description:
Infants who consulted after the implementation of the pre-convention, who consulted between January 1st 2010 and December 31st 2021. Inclusion criteria: * Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2010 and the 31st of December 2021 and receiving the label "feeding difficulties". * The infants have a pediatric feeding disorder that prevent them from feeding normally by oral means. * The infants need or have needed (enteral or parenteral) artificial nutrition. * The infants are aged between 0 and 12 years at their first presentation. * The infants are capable of developing normal feeding behavior. Infants will be excluded from this study if they: * Have no 6-months follow-up available. * Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.
Treatment:
Combination Product: Structured multi-disciplinary approach

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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