Clin2
NCT07775066Possibly a fitNot yet recruiting

Measuring AFP levels in children with acute flaccid paralysis

Acute Flaccid ParalysisAFPGullian Barre SyndromeTransverse Myelitis

Part of Brain & nervous system, Cancer, Immune system & allergy, Infections clinical trials.

This trial is studying a protein called AFP in children with sudden muscle weakness (acute flaccid paralysis). It aims to see if AFP levels help understand the condition better.

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

Phase
N/A
Enrollment
30 people
Ages
1 month to 16 years
Study type
Observational

Who can take part

  • Child must be between 1 month and 16 years old.
  • Child must be admitted to the pediatric emergency or intensive care unit.
  • Child must have or be suspected of having acute flaccid paralysis (sudden muscle weakness or limpness).
  • The paralysis must be due to a neurological (nerve) cause, not a muscle or joint issue.
  • Complete medical records must be available.

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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