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APRT Deficiency clinical trials

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NCT ID: NCT02026388 Recruiting - Clinical trials for Primary Hyperoxaluria

Rare Kidney Stone Consortium Biobank

Start date: May 2013
Phase:
Study type: Observational

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.

NCT ID: NCT00588562 Recruiting - Clinical trials for Primary Hyperoxaluria

Rare Kidney Stone Consortium Patient Registry

RKSC
Start date: July 2003
Phase:
Study type: Observational

The purpose of this study is to collect medical information from a large number of patients in many areas of the world with primary hyperoxaluria (PH), Dent disease, Cystinuria and APRT deficiency. This information will create a registry that will help us to compare similarities and differences in patients and their symptoms. The more patients we are able to enter into the registry, the more we will be able to understand the Primary Hyperoxalurias,Dent disease, cystinuria and APRT and learn better ways of caring for patients with these diseases.