Rare Kidney Stone Consortium Biobank

Status Recruiting

Clinical Trial Summary

This study is being done to obtain samples from patients with primary hyperoxaluria, cystinuria, adenine phosphoribosyl transferase (APRT) deficiency, and Dent disease, and from their family members, for use in future research.

Clinical Trial Description

Biologic samples will be stored in the biobank from well characterized patients with primary hyperoxaluria, cystinuria, APRT deficiency, and Dent disease, and from their family members, for use in future research. This will help to advance our understanding of disease expression and the factors associated with kidney injury in these four diseases with the overall goal of developing new treatments to preserve kidney function and reduce nephrocalcinosis and stone formation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02026388
Study type	Observational
Source	Mayo Clinic
Contact	Barb M Seide
Phone	507-255-0387
Email	seide.barbara@mayo.edu
Status	Recruiting
Phase
Start date	May 2013
Completion date	June 2025

View Details

See also
Status	Clinical Trial	Phase
Withdrawn	`NCT00875823` - International Registry for Primary Hyperoxaluria	N/A
Recruiting	`NCT05687474` - Baby Detect : Genomic Newborn Screening
Completed	`NCT02340689` - Primary Hyperoxaluria Mutation Genotyping/Phenotyping
Completed	`NCT00638703` - Study to Evaluate the Efficacy and Safety of OxabactTM on Reduction of Urinary Oxalate in Primary Hyperoxaluria Patients	Phase 2/Phase 3
Recruiting	`NCT06065852` - National Registry of Rare Kidney Diseases
Completed	`NCT03819647` - Evaluation of the Efficacy of Stiripentol (Diacomit) as Monotherapy for the Treatment of Primary Hyperoxaluria	Phase 2
Completed	`NCT02000219` - Study to Evaluate the Efficacy and Safety of Oxabact (OC5) in Primary Hyperoxaluria Patients Who Are on Dialysis	Phase 2
Recruiting	`NCT05843851` - Genetic Newborn Screening for Cystinosis and Primary Hyperoxaluria	N/A
Recruiting	`NCT00588562` - Rare Kidney Stone Consortium Patient Registry
Completed	`NCT03391804` - Study of ALLN-177 in Patients Aged 12 Years or Older With Enteric or Primary Hyperoxaluria and Hyperoxalemia	Phase 2
Completed	`NCT03116685` - A Study to Evaluate the Efficacy and Safety of Oxabact in Patients With Primary Hyperoxaluria	Phase 3
Recruiting	`NCT05107830` - Phenotyping of Primary Hyperoxaluria
Active, not recruiting	`NCT04152200` - A Study to Evaluate Lumasiran in Patients With Advanced Primary Hyperoxaluria Type 1	Phase 3
Recruiting	`NCT05001269` - Nedosiran in Pediatric Patients From Birth to 11 Years of Age With PH and Relatively Intact Renal Function	Phase 2
Completed	`NCT03392896` - Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria	Phase 1
Completed	`NCT02012985` - Study to Evaluate the Efficacy and Safety of Oxabact (OC5) in Patients With Primary Hyperoxaluria	Phase 1/Phase 2
Completed	`NCT01037231` - Phase 2/3 Oxabact Study	Phase 2/Phase 3
Completed	`NCT00589225` - Primary Hyperoxaluria Mutation Genotyping	Phase 1
Completed	`NCT02124395` - Health-related Quality of Life in Rare Kidney Stone
Completed	`NCT03350451` - An Extension Study of an Investigational Drug, Lumasiran (ALN-GO1), in Patients With Primary Hyperoxaluria Type 1	Phase 2