Original Query: ALL
Previous Study | Return to List | Next Study

Primary Hyperoxaluria Mutation Genotyping

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00589225
Recruitment Status : Completed
First Posted : January 9, 2008
Last Update Posted : July 7, 2016
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Oxalosis and Hyperoxaluria Foundation (OHF)
Information provided by (Responsible Party):
Dawn S. Milliner, M.D., Mayo Clinic

No Study Results Posted on for this Study
  Recruitment Status : Completed
  Primary Completion Date : September 2014
  Study Completion Date : September 2014