About the Study

Hemodialysis Registry: A tool used to collect health information on children receiving hemodialysis for future research

The purpose of this research study is to continuously monitor outcomes in children around the world that are on hemodialysis. This registry should provide much needed information to doctors, nurses, dieticians, psychologists, social workers, and health care administrators, and help improve the wellbeing of children currently on HD. Being in this study involves having data collected from the child's medical record by a study team member and entered into an international database (registry). The data to be entered will include the child's date of birth, a unique study number, dates of service, and relevant medical information.

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Full Study Name: IPHN - Data entry registry for patients on hemodialysis