Clin2
NCT01668186Worth exploringRecruiting

Study of how peroxisome disorders change over time

Peroxisome Biogenesis DisorderZellweger Spectrum DisorderRCDP - Rhizomelic Chondrodysplasia PunctataD-Bifunctional Protein DeficiencyAlpha-Methylacyl-CoA Racemase DeficiencyPeroxisomal Acyl-CoA Oxidase DeficiencyPeroxisomal Acyl-CoA Oxidase 2 DeficiencyATP Binding Cassette Subfamily D Member 3 Gene Mutation

Part of Bones, joints & muscles, Brain & nervous system, Digestive system, Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.

This study follows people with peroxisome biogenesis disorders (PBD) or closely related enzyme/protein defects to learn how symptoms and health changes over time. It may help researchers better understand the condition and plan future treatments.

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

Phase
N/A
Enrollment
244 people
Ages
Any age
Study type
Observational

Who can take part

  • You have been diagnosed with a peroxisome biogenesis disorder (PBD), or
  • You have a single peroxisome enzyme or protein defect that acts like PBD.
  • You must not be diagnosed with a condition that is not PBD or similar.
  • You must not have a peroxisome problem that does not match the PBD-like pattern.

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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