Data Registry

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The Data Registry for various types of cardiovascular disease is being set up and running. The SRCMRC clinical registry working group was founded in 2015 for the purpose of systematically collecting patient information in order to achieve a predetermined scientific, clinical or policy goal. Its mission was to establish a platform for researchers to launch registries. Firstly, we have evaluated our actual and also needed resources for this purpose. Then with the help of national and international experts, several workshops run to increase the scientific and technical knowledge regarding clinical registries.

Meanwhile the result of the priorities survey which is collecting from our faculties lead to establish following registries:

  • Infective endocarditis
  • Atrial fibrillation
  • NSTEMI
  • Acute heart failure
  • Acute aortic dissection
  • Critical limb ischemia
  • Pulmonary hypertension
  • Tetralogy of  Fallot
  • Cardiomyopathy, myocarditis and amyloidosis
  • Pregnancy and cardiac disease
  • Cardio-oncology

 

At the beginning the patients’ information gathered along with electronic hospital records. Soon after that a separate database with the name of “Regitory” was born for the registries. Regitory is a web-based database with the ability of data entry, data saving and also data analysis.

 

Last Update At : 27 September 2020