Oxalate Excretion Profile in Patients With a Heterozygous Mutation of the AGXT (Alanine-glyoxylate Aminotransferase) Gene
NCT06283082
·
clinicaltrials.gov ↗
NA
Phase
COMPLETED
Status
25
Enrollment
OTHER
Sponsor class
Conditions
Hyperoxaluria (Disorder)
Interventions
DIAGNOSTIC_TEST:
Lithiasis assessment
Sponsor
Hospices Civils de Lyon