Plain-English translation of NCT06471842 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This research is studying how common eating and feeding difficulties are in children with inherited metabolic diseases—rare genetic conditions that require special diets to manage. Researchers want to understand whether these eating challenges happen more often in some types of these diseases than others, so that doctors can spot and help affected children earlier and better.
Right now, doctors don't have clear information about how many children with these genetic metabolic diseases struggle with eating and feeding. By measuring this, the study hopes to raise awareness and help hospitals provide better, earlier care for children facing these challenges.
You likely qualify if…
You likely don't qualify if…
You and your child would come for a single hospital visit as part of your regular medical care. During the visit, a therapist or dietitian would ask you questions using a standardized assessment tool and collect information from your child's medical records—the whole process happens in one appointment. No extra hospital visits beyond your normal check-ups would be needed.
AI-generated summary from trial data · Jun 8, 2026 · Not medical advice
France
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
URC-CIC Paris Descartes Necker Cochin
Enrollment target
~200 participants
Started
August 2024
Primary completion
August 2026
This trial's estimated completion date has passed — the record may not be fully up to date.
Age range
12 Months – 6 Years
Last updated on clinicaltrials.gov in November 2025.
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Central contact
Manon Tessier
Assistance Publique - Hôpitaux de Paris
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.