Clin2
NCT01401998Possibly a fitRecruiting

Study collecting information from people with ARPKD

Hepato/Renal Fibrocystic DiseaseAutosomal Recessive Polycystic Kidney DiseaseJoubert SyndromeBardet Biedl SyndromeMeckel-Gruber SyndromeCongenital Hepatic FibrosisCaroli SyndromeOro-Facial-Digital Syndrome Type I

Part of Brain & nervous system, Digestive system, Eyes & vision, Genetic & congenital, Kidney & urinary, Women’s health & pregnancy clinical trials.

This study looks at medical records, imaging, and genetic testing for people with autosomal recessive polycystic kidney disease (ARPKD). It may help researchers better understand the condition and how it affects the liver and kidneys.

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

Phase
N/A
Enrollment
200 people
Ages
Up to 18 years
Study type
Observational

Who can take part

  • You (or your child) have ARPKD confirmed by a history, scan, tissue sample, exam after death, or genetic test
  • Your ARPKD affects the liver and/or kidneys with scarring and cyst-type changes
  • You do not have urinary tract birth defects (urinary tract malformations)
  • You do not have major birth defects in other body systems

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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