Clinical Trials

Showing trials with last updates posted in 2023.

NCT06065852 | RECRUITING
35000 participants

National Registry of Rare Kidney Diseases

Study Type:
OBSERVATIONAL
Last Updated:
2023-10-04
Start Date:
2009-11-06
Completion:
2039-12-31
Conditions
  • Adenine Phosphoribosyltransferase Deficiency
  • AH Amyloidosis
  • AHL Amyloidosis
  • AL Amyloidosis
  • Alport Syndrome
  • Atypical Hemolytic Uremic Syndrome
  • Autoimmune Distal Renal Tubular Acidosis
  • Autosomal Recessive Proximal Renal Tubular Acidosis
  • Autosomal Recessive Distal Renal Tubular Acidosis
  • Autosomal Dominant Polycystic Kidney Disease
  • Autosomal Recessive Polycystic Kidney Disease
  • Bartter Syndrome
  • BK Nephropathy
  • C3 Glomerulopathy With Monoclonal Gammopathy
  • C3 Glomerulopathy
  • Calciphylaxis
  • Crystalglobulinaemia
  • Crystal-storing Histiocytosis
  • Cystinosis
  • Cystinuria
  • Dense Deposit Disease
  • Dent Disease
  • Denys-Drash Syndrome
  • Dominant Hypophosphataemia With Nephrolithiasis and/or Osteoporosis
  • Drug Induced Fanconi Syndrome
  • Drug-Induced Hypomagnesemia
  • Drug-Induced Nephrogenic Diabetes Insipidus
  • Epilepsy, Ataxia, Sensorineural Deafness and Tubulopathy
  • Fabry Disease
  • Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis
  • Familial Primary Hypomagnesemia With Hypocalcuria
  • Familial Primary Hypomagnesaemia With Normocalciuria
  • Familial Renal Glucosuria
  • Fanconi Renotubular Syndrome 1
  • Fanconi Renotubular Syndrome 2
  • Fanconi Renotubular Syndrome 3
  • Fibrillary Glomerulonephritis
  • Fibromuscular Dysplasia
  • Focal Segmental Glomerulosclerosis
  • Generalised Pseudohypoaldosteronism Type 1
  • Gitelman Syndrome
  • Heavy-Metal-Induced Fanconi Syndrome
  • Hepatocyte Nuclear Factor 1-Beta-Associated Monogenic Diabetes
  • Hereditary Renal Hypouricemia
  • Hereditary Hypophosphatemic Rickets With Hypercalciuria
  • Hyperuricaemic Nephropathy
  • IgA Nephropathy
  • Immunotactoid Glomerulonephritis With Organised Microtubular Mononoclonal Immunoglobulin Deposits
  • Inherited Renal Cancer Syndromes
  • Intracapillary Monoclonal IgM Without Cryoglobulin
  • Intraglomerular/Capillary Lymphoma/Leukaemia
  • Isolated Autosomal Dominant Hypomagnesaemia Glaudemans Type
  • Liddle Syndrome
  • Light Chain Cast Nephropathy
  • Light Chain Proximal Tubulopathy Without Crystals
  • Light Chain Proximal Tubulopathy With Crystals
  • Lowe Syndrome
  • Membranous Nephropathy
  • Membranoproliferative Glomerulonephritis
  • Medullary Cystic Kidney Disease
  • Minimal Change Nephropathy
  • Mitochondrial Disease Of The Kidney
  • Monoclonal Immunoglobulin Deposition Disease
  • Nail Patella Syndrome
  • Nephrogenic Diabetes Insipidus
  • Nephrogenic Syndrome of Inappropriate Antidiuresis
  • Nephronophthisis
  • Primary Hypomagnesemia With Secondary Hypocalcemia
  • Primary Hyperoxaluria
  • Proliferative Glomerulonephritis With Monoclonal IgG Deposits
  • Proximal Tubulopathy Without Crystals
  • Pseudohypoaldosteronism Type 1, 2A-2E
  • Pure Red Cell Aplasia
  • Retroperitoneal Fibrosis
  • Sickle Cell Nephropathy
  • Shiga Toxin Associated Haemolytic Uraemic Syndrome
  • Steroid Resistant Nephrotic Syndrome
  • Steroid-Sensitive Nephrotic Syndrome
  • Thin Basement Membrane Nephropathy
  • Thrombotic Microangiopathy With Monoclonal Gammopathy
  • Type 1 Cryoglobulinaemic Glomerulonephritis
  • Tuberous Sclerosis
  • Unclassified Monoclonal Gammopathy Of Renal Significance
  • Vasculitis
No Results Yet
Previous
Sorted by latest updates
Next
Showing 40 trials per page