A non-interventional, national longitudinal multicenter study of CV secondary prevention in Tunisia
The NATURE-STOP-CHD study is carried out in Tunisia at cardiology consultations in hospitals and in the liberal sector. The study is a longitudinal non-interventional registry of patient undergoing secondary CV prevention. The data collected are managed by the DACIMA Clinical Suite® platform, which complies with international standards: FDA 21 CFR part 11 (Food and Drug Administration 21 Code of Federal Regulations part 11), HIPPA (Health Insurance Portability and Accountability Act), ICH (International Conference on Harmonisation), MedDRA (Medical Dictionary for Regulatory Activities). The DACIMA Clinical Suite® platform allows to track the data entered, check for inconsistencies and missing data, and schedule monitoring visits. A Steering Committee is set up to monitor patient inclusions, verify data sources, perform audit trails and prepare the statistical analysis plan for the study.
Study Type
OBSERVATIONAL
Enrollment
5,000
Tunisian Society of Cardiology and Cardiovascular Surgery
Tunis, Tunisia
RECRUITINGCompliance
Number of subjects with sufficient adherence to their cardiovascular medication
Time frame: From enrollment to the end of the follow-up (12 months)
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