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Clinical Trial Summary

The National Tunisian Registry of Cardiac Implantable Electronic Devices is an observational, prospective and multicenter study aiming to assess the epidemiological, clinical and therapeutic profile of cardiac implantable electronic Devices in Tunisia. Cardiologists from both sectors (public and private) are participating in the study, with 26 investigational centers. Data is captured electronically by DACIMA Clinical Suite, according to FDA 21 CFR part 11 (Food and Drug Administration 21 Code of Federal Regulations part 11), HIPAA (Health Insurance Portability and Accountability Act) & ICH (International Conference on Harmonisation) requirements.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Cardiac Implantable Electronic Devices

NCT number NCT05361759
Study type Observational [Patient Registry]
Source Dacima Consulting
Contact
Status Completed
Phase
Start date January 18, 2021
Completion date August 15, 2023

See also
  Status Clinical Trial Phase
Completed NCT04389697 - Fasting Versus Non-Fasting for Cardiac Implantable Electronic Devices (FastCIED Study) N/A