- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02142270
Epidemiology of Sudden Cardiac Arrest in Sub-Saharan Africa: Rationale and Design
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Aime Bonny
- Phone Number: 33637975227
- Email: aimebonny@yahoo.fr
Study Locations
-
-
-
Douala, Cameroon, 2701
- Bonny
-
Principal Investigator:
- Aime Bonny, MD
-
Contact:
- Aime Bonny
- Phone Number: 33637975227
- Email: aimebonny@yahoo.fr
-
Sub-Investigator:
- Rene Fongang
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
All residents of districts of interest will be surveyed during 3 years. premature deaths occurring in residents of districts of interest will be checked for past medical history, circumstances of death, and autopsy report (if possible). Investigators will also analyze the employment of resuscitation attempts during the timeframe of sudden cardiac arrest (SCA) in various patient populations throughout African countries.
The arm group of the study is every resident of the district of interest
Description
Inclusion Criteria:
- Victims of cardiac arrest, either SCD or aborted SCA
Exclusion Criteria:
- Age ≤ 15 years.
- Refusal of consent (by the family).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Victims of cardiac arrest, either SCD or aborted SCA
|
Premature death
All residents of districts of interest will be surveyed during 3 years. premature deaths occurring in residents of districts of interest will be checked for past medical history, circumstances of death, and autopsy report (if possible). Investigators will also analyze the employment of resuscitation attempts during the timeframe of sudden cardiac arrest (SCA) in various patient populations throughout African countries. The arm group of the study is every resident of the district of interest |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Sudden Cardiac Death
Time Frame: 3 years
|
3 years
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PASCAR
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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