- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05869214
Middle East African Registry Women CardioVascular Disease (MEA-WCVD)
May 11, 2023 updated by: Tunisian Society of Cardiology and Cardiovascular Surgery
The MEA cardiology societies have joined forces to tackle the issue by establishing a tangible real-world data registry in every MEA country.
This endeavor has resulted in the development of a multicenter registry called MEA-WCVD, which is being sponsored by each national cardiology society from participating countries.
All data gathered will be consolidated into a singular registry for thorough analysis.
Country specific analysis will be performed.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Anticipated)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Salem Abdessalem, Dr
- Email: salem.abdesselem@gmail.com
Study Contact Backup
- Name: Selma Charfeddine, dr
- Email: selma_charfeddine@yahoo.fr
Study Locations
-
-
-
Sfax, Tunisia
- Recruiting
- Hedi chaker Hospital
-
Contact:
- Selma Charfeddine, dr
- Email: selma_charfeddine@yahoo.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
All patients having their consultation in the study participating site.
Description
Inclusion Criteria:
- All incomers in Cardiovascular (CV) diseases in hospital or out hospital facilities with one of the 4 diagnosis (Heart Failure (HF), Atrial fibrillation (AF), Valvular Heart disease (VHD), ischemic heart disease (IHD)
- Age over 18 years old
- Men and Women
- Signature of consent form
Exclusion Criteria:
Patients with diseases other than the 4 previously mentioned in inclusion criteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Cardiovascular diseases care management in women will be compared to men in MEA countries according to current practice guidelines
Time Frame: 2 months
|
2 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Identify inequalities between both genders in terms of: • Healthcare insurance • Incomes • Access to healthcare
Time Frame: 2 months
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 10, 2023
Primary Completion (Anticipated)
July 10, 2023
Study Completion (Anticipated)
July 10, 2023
Study Registration Dates
First Submitted
May 11, 2023
First Submitted That Met QC Criteria
May 11, 2023
First Posted (Actual)
May 22, 2023
Study Record Updates
Last Update Posted (Actual)
May 22, 2023
Last Update Submitted That Met QC Criteria
May 11, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WCVD012023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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