- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03819452
Impact of Vitamin D on Acute Ischemic Stroke Prognosis (IVASTO)
January 25, 2019 updated by: Abha International Private Hospital
This is a registry for all patients admitted to hospital settings with Ischemic stroke in Mansoura University Hospital.
The registry will capture patients' data, investigations and vitamin D level on admission.
Follow-up is taking place using MODIFIED RANKIN SCALE
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
59
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Dakahlia
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Mansourah, Dakahlia, Egypt
- Mansoura University
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-
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Basel, Switzerland, 7415
- IQVIA
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients attending to hospital settings diagnosed with ischemic stroke are investigated to have low level of vitamin D
Description
Inclusion Criteria:
- Newly diagnosed ischemic stroke not older than 48 hours
Exclusion Criteria:
- Ischemic stroke due to accidents or any trauma
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
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Correlation of Vitamin D level and the Incidence of Ischemic Stroke
Time Frame: On admission
|
Correlation Analyses between vitamin D and ischemic stroke will be applies
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On admission
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
impact of vitamin D on ischemic stroke in relationship with gender
Time Frame: On admission
|
subgroup analyses per gender will be applied to check the difference of vitamin D
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On admission
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Mohamed FLeifel, MD PhD, Abha International Private Hospital
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)
August 1, 2018
Primary Completion (Actual)
January 25, 2019
Study Completion (Actual)
January 25, 2019
Study Registration Dates
First Submitted
January 25, 2019
First Submitted That Met QC Criteria
January 25, 2019
First Posted (Actual)
January 28, 2019
Study Record Updates
Last Update Posted (Actual)
January 28, 2019
Last Update Submitted That Met QC Criteria
January 25, 2019
Last Verified
January 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Pathologic Processes
- Necrosis
- Cardiovascular Diseases
- Vascular Diseases
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Brain Ischemia
- Infarction
- Brain Infarction
- Stroke
- Ischemic Stroke
- Ischemia
- Cerebral Infarction
- Physiological Effects of Drugs
- Micronutrients
- Vitamins
- Bone Density Conservation Agents
- Vitamin D
Other Study ID Numbers
- Fleifel002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
Data of study participants will be kept confidential and no intention for distribution.
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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