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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03085576
Other study ID # DAC-001-NATUREAF
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2017
Est. completion date July 30, 2018

Study information

Verified date April 2021
Source Dacima Consulting
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A non-interventional, national longitudinal study of atrial fibrillation performed with 91 cardiologists.


Description:

The NATURE-AF study is carried out in Tunisia at cardiology consultations in hospitals and in the liberal sector. A total of 91 cardiologists participate in the selection of patients as investigators. The study is a longitudinal non-interventional registry of atrial fibrillation. 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.


Recruitment information / eligibility

Status Completed
Enrollment 910
Est. completion date July 30, 2018
Est. primary completion date May 30, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - At least one episode of atrial fibrillation, documented on a 12-lead ECG and / or a rhythmic holter (duration of the episode: 30 seconds or more) - Recent atrial fibrillation diagnosed for less than a year - Regular monitoring every 3 months is ensured - Informed, read and signed consent Exclusion Criteria: - Estimated life expectancy at less than 12 months - Transient atrial fibrillation due to reversible cause (eg acute myocardial infarction, following cardiac surgery, acute alcohol intoxication, hyperthyroidism, pulmonary embolism or other acute pulmonary disease, pericarditis, myocarditis, hydro-electrolyte disorder, metabolic disorder) - Cardiac surgery = 3 months - Atrial flutter isolated without atrial fibrillation - Mental disorders - Ongoing anticoagulation for reasons other than atrial fibrillation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Tunisia STCCCV - Société Tunisienne de Cardiologie et de Chirurgie Cardio-Vasculaire Tunis

Sponsors (2)

Lead Sponsor Collaborator
Dacima Consulting Société Tunisienne de Cardiologie & de Chirurgie Cardio-Vasculaire

Country where clinical trial is conducted

Tunisia, 

References & Publications (2)

Ben Halima A, Ouali S, Mourali MS, Chabrak S, Chettaoui R, Ben Halima M, Haggui A, Larbi N, Krichène S, Marrakchi S, Kacem S, Chrigui R, Abbes MF, Baccar H, Baraket N, Ben Halima N, Ben Khalfallah A, Ben Mbarek M, Ben Youssef S, Boughzala E, Boujnah MR, Drissa H, Gamra H, Gasmi A, Haouala H, Harrath Y, Issa I, Jeridi G, Kachboura S, Kammoun S, Kraiem S, Maatouk F, Milouchi S, Nasraoui W, Neji A, Sayahi K, Sdiri W, Smati W, Tlili S, Abid L, Abdesselem S, Zakhama L, Mahdhaoui A, Kammoun H, Ben Omrane S, Addad F. Design and Rationale of the National Tunisian Registry of Atrial Fibrillation: Protocol for a Prospective, Multicenter Trial. JMIR Res Protoc. 2018 Oct 15;7(10):e181. doi: 10.2196/resprot.8523. — View Citation

Ouali S, Ben Halima A, Chabrak S, Chettaoui R, Ben Halima M, Haggui A, Krichane S, Noureddine L, Marrakchi S, Charfeddine S, Hassine M, Sayahi K, Abbes Mohamed F, Nasraoui W, Ajmi H, Ben Miled M, Jebbari Z, Meghaieth MA, Allouche E, Mechmeche R, Zakhama L, Sdiri W, Ben Khalfallah A, Gharbi A, Milouchi S, Neji A, Antit S, Battikh K, Drissa M, Kaabachi S, Najar T, Tlili R, Chahbani I, Charfeddine H, Ben MM, Braham S, Maatouk F, Abdesselem S, Ayari M, Garbaa R, Hamrouni N, Mbarek D, Rekik H, Zaghdoudi H, Ayadi W, Baraket F, Ben Brahim K, Ben Romdhane M, Bousadia H, Brahim W, Mezri M, Guesmi A, Ounissi T, Kammoun S, Smati W, Tlili S, Zoughi K, Zemni J, Cheikh Bouhlel M, Islem S, Jemli R, Joulak A, Mzoughi K, Naanea H, Hached L, Hadrich M, Hmem M, Kacem S, Kammoun I, Othmani R, Ouerghi A, Abid S, Ennouri R, Haidar S, Heraiech S, Jammali M, Jarrar M, Riahi L, Trimech B, Azaiez MA, Azzouzi F, Ben Jemaa K, Ben Rejab O, Chrigui R, Wechtati W, Boughzela E, Jridi G, Bezdah L, Kraiem S, Drissa H, Ben Youssef S, Fehri W, Kachboura S, Gamra H, Kammoun S, Mourali MS, Addad F, Abid L. Epidemiological characteristics, management, and outcomes of atrial fibrillation in TUNISIA: Results from the National Tunisian Registry of Atrial Fibrillation (NATURE-AF). Clin Cardiol. 2021 Apr;44(4):501-510. doi: 10.1002/clc.23558. Epub 2021 Mar 11. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of stroke or transient ischemic attack, thromboembolic events and cardiovascular death Number of patients with ischemic stroke and/or transient ischemic attack, and/or arterial embolization during the follow-up period Every 3 months up to 1 year
Secondary Haemorrhagic accidents All bleeding events (digestive, cerebral, other locations) Every 3 months up to 1 year
Secondary Measurement of INR (International Normalized Ratio) INR measurement of venous blood sampling Every month for 1 year
Secondary TTR (percent Time in Therapeutic INR Range) The mean TTR obtained in patients who received anticoagulant therapy 1 year
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