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Hyperoxaluria, Primary clinical trials

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NCT ID: NCT00875823 Withdrawn - Kidney Stones Clinical Trials

International Registry for Primary Hyperoxaluria

Start date: September 2003
Phase: N/A
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. This medical information will be entered into a registry to help the investigators compare similarities and differences in patients and their symptoms. The more patients that the investigators are able to enter into the registry, the more the investigators will be able to understand primary hyperoxaluria and learn better ways of treating patients with this disease. It is the investigators hope that by entering as many patients with PH as possible, the information that the investigators collect may help physicians diagnose patients sooner and determine what treatments may work best on patients with similar medical or genetic backgrounds.

NCT ID: NCT00280215 Withdrawn - Hyperoxaluria Clinical Trials

Renal Protective Effect of ACEI and ARB in Primary Hyperoxaluria

Start date: December 2007
Phase: Phase 3
Study type: Interventional

This study will test the effectiveness of two medications: ACEI (angiotensin converting enzyme inhibitor)and ARB (angiotensin receptor blocker) in reducing the renal injury induced by hyperoxaluria in patients with Primary Hyperoxaluria. Hypothesis: Calcium oxalate crystal deposition in the kidney causes inflammation and resulting injury to kidney tissue. Angiotensin blockade will improve these changes, thus slowing the progression of renal insufficiency in patients with Primary Hyperoxaluria.