Kidney Stones Clinical Trial
Official title:
International Registry for Hereditary Calcium Stone Diseases
Verified date | April 2015 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
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.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | July 2009 |
Est. primary completion date | July 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Liver biopsy or genetic analysis that confirms a diagnosis of hyperoxaluria - In the absence of a liver biopsy: - Urine oxalate excretion of >0.8 mmol/1.73 m² /day without other causes such as enteric hyperoxaluria - Family history of PH in a sibling will be supportive - A history or current finding of kidney stones or nephrocalcinosis will be supportive - An increase in urine glycolate may suggest PHI or an increase in urine L-glycerate may suggest PHII, though not required for diagnosis. - Patients presenting in renal failure with an elevate pre-dialysis plasma oxalate of 60 umol/l and a kidney biopsy that confirms extensive oxalate deposition, or evidence of systemic oxalosis Exclusion Criteria: - Patients without any of the above or a confirmed diagnosis of PH |
Observational Model: Cohort, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
United States | Children's Memorial Hospital | Chicago | Illinois |
United States | Mattel Children's Hospital at UCLA | Los Angeles | California |
United States | Mayo Clinic Rochester | Rochester | Minnesota |
United States | University of California at Davis | Sacramento | California |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic | National Institutes of Health (NIH), Oxalosis and Hyperoxaluria Foundation (OHF) |
United States,
Lieske JC, Monico CG, Holmes WS, Bergstralh EJ, Slezak JM, Rohlinger AL, Olson JB, Milliner DS. International registry for primary hyperoxaluria. Am J Nephrol. 2005 May-Jun;25(3):290-6. Epub 2005 Jun 15. — View Citation
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