Clin2
NCT06065852Possibly a fitRecruiting

National registry for rare kidney diseases

Adenine Phosphoribosyltransferase DeficiencyAH AmyloidosisAHL AmyloidosisAL AmyloidosisAlport SyndromeAtypical Hemolytic Uremic SyndromeAutoimmune Distal Renal Tubular AcidosisAutosomal Recessive Proximal Renal Tubular Acidosis

Part of Blood & lymphatic, Bones, joints & muscles, Brain & nervous system, Cancer, Genetic & congenital, Heart & circulation, Hormones & metabolism, Immune system & allergy, Kidney & urinary, Skin, Women’s health & pregnancy clinical trials.

This study creates a registry to collect health information from people with rare kidney diseases. It aims to improve understanding and future treatments by tracking patient experiences.

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

Phase
N/A
Enrollment
35,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You or your child has a rare kidney disease
  • All ages can join, from children to adults
  • Each rare disease has its own specific rules for joining
  • You must be willing to share your health information

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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