Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07034274

National Tunisian Clinical Registry on CardioVascular Secondary Prevention Clinical

Status
Recruiting
Phase
Study type
Observational
Enrollment
5,000 (estimated)
Sponsor
Dacima Consulting · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

A non-interventional, national longitudinal multicenter study of CV secondary prevention in Tunisia

Detailed description

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.

Conditions

Timeline

Start date
2025-06-09
Primary completion
2025-07-31
Completion
2025-07-31
First posted
2025-06-24
Last updated
2025-06-24

Locations

1 site across 1 country: Tunisia

Source: ClinicalTrials.gov record NCT07034274. Inclusion in this directory is not an endorsement.

National Tunisian Clinical Registry on CardioVascular Secondary Prevention Clinical (NCT07034274) · Clinical Trials Directory