- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07298668
Cardiovascular Risk Factors in Middle Eastern Patients With Stroke (JoSMMART)
Standard Modifiable Risk Factors in Middle Eastern Patients With Stroke (Jo-SMMART Study)
Study Overview
Status
Detailed Description
Stroke is a well-known a leading cause of death and disability in the Middle East. There remain many knowledge gaps in evaluating the prevalence of risk factors among patients with stroke in the Middle East. Unravelling the impact of these risk factors and controlling them can positively lower the incidence of stroke. Disparities in stroke risk factors, may well be related to ethnicity of the Middle Eastern populations , will be compared with those among stroke patients in the western literature.
These clinically relevant issues have not been studied extensively in the Middle East where most of the studies in atherosclerotic cardiovascular disease have focused on acute coronary syndrome more than stroke. Exploring new information on risk factors of stroke in this region that helps fill some of the knowledge gaps.
Stroke has been attributed, in the majority of cases, to the traditional four standard modifiable risk factors of hypertension, type 2 diabetes, dyslipidemia, and cigarette smoking. However, ethnicity and geography account for the interregional differences of the prevalence of risk factors in patients with stroke.
The Jo-SMMART ill evaluate risk factors in 2000 stroke patients in Jordan as a representative of the Middle Eastern population, the prevalence of those with none of the 4 risk factors and the differences in clinical profiles and demographic features on those with risk factors and those with no risk factors. Lipid profile and use of lipid lowering agents will also be evaluated, and furthermore the die0fferneces between young vs old, and men vs women stroke patients ill be addressed.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Ayman Hammoudeh, MD, FACC
- Phone Number: 065001000
- Email: hammoudeh_ayman@yahoo.com
Study Contact Backup
- Name: Laith Habahbeh, MD
- Phone Number: 065001000
- Email: a.hammoudeh@istisharihospital.com
Study Locations
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Amman, Jordan, 11184
- Istishari Hospital
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Contact:
- Laith Habahbeh, MD
- Phone Number: 065001000
- Email: hammoudeh_ayman@yahoo.com
-
Contact:
- Ayman Hammoudeh, MD, FACC, FSCAI
- Phone Number: 065001000
- Email: hammoudeh_ayman@yahoo.com
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diagnosis of stroke upon admission to the hospital
- Adult aged 18 years or older
- Available lipid profile on hospital admission
Exclusion Criteria:
- Stroke diagnosis unconfirmed
- age younger than 18 years
- No available lipid profile on admission
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of hypertension in stroke patients (survey interview)
Time Frame: Baseline
|
BP more 140/90 or known diagnosis of high blood pressure or patient already on blood pressure medication
|
Baseline
|
|
Prevalence of type 2 diabetes in stroke patients (survey interview)
Time Frame: BASELINE
|
HbA1c more than 6.5%, or known diagnosis of type 2 diabetes or patient already on anti diabetes medications
|
BASELINE
|
|
Prevalence of elevated serum level of low density lipoprotein cholesterol in stroke patients (survey interview)
Time Frame: BASELINE
|
Elevated serum level of low density lipoprotein cholesterol > 55 mg/dl or patient already on lipid lowering medication
|
BASELINE
|
|
Prevalence of current cigarette smoking in stroke patients (survey interview)
Time Frame: BASELINE
|
Known current cigarette smoking of any number of cigarettes per day
|
BASELINE
|
|
Use of lipid lowering therapy (survey interview)
Time Frame: BASELINE
|
Current use of statin, ezitimibe, PCS9 inhibitor of small interfering RNA agent to lower the LDL-C
|
BASELINE
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- JOCVA1.NOV2025/2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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