The creation of a patient’s database would also allow researchers to track certain diseases as well as to patients' responses to certain drugs.
The emphasis is on experimental results relevant to quantitative renal physiology, with a particular focus on data relevant for evaluation of parameters in statistical models of renal function.
CDKD currently contains more than 10,000 data entries. In an effort to reduce human error and paper work. CDKD is a step to make as much as possible data easily accessible to scientific community. Each patient's record is unique and identified with the patient's case id and Identification number.