Clin2
NCT07006207Worth exploringNot yet recruiting

Smell and brain pathways in Prader-Willi syndrome

Prader-Willi Syndrome

Part of Brain & nervous system, Genetic & congenital, Hormones & metabolism clinical trials.

This study looks at how the brain handles smells in children with Prader-Willi syndrome. By comparing brain images and smell test results, it may help understand the condition better.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
30 people
Ages
5 years to 7 years
Study type
Interventional

Who can take part

  • Your child has a confirmed genetic diagnosis of Prader-Willi syndrome, and the specific genetic type has been identified.
  • Your child is between 5 and 7 years old.
  • Your child is already scheduled for a hospital stay at the reference center in Toulouse.
  • Your child can have an MRI safely (no metal implants, no allergy to MRI contrast, etc.).
  • Your child has no allergy to the smells used in the smell test.
  • Your child does not have a cold, sinus infection, or other nasal blockage on the day of the test.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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