SERUM VITAMIN B12 LEVELS IN PATIENTS WITH HEMORRHAGIC VS ISCHEMIC CEREBROVASCULAR EVENT. (ViBEVC)

December 19, 2023 updated by: Hiram Jaramillo Ramirez, Hospital General de Mexicali
Cerebral vascular events (CVA) have a high prevalence in our environment; they are the first cause of disability and the second cause of death in the world (6.6 million deaths). 71% of all strokes worldwide correspond to the ischemic type, which is defined as an infarction in the brain, spinal cord or retina; The remaining 10-40% are hemorrhagic and are due to rupture of cerebral arteries. Until epidemiological week 35 of 2022, 34,643 cases were reported in Mexico, for this week in 2021, 26,462 cases had been reported. Baja California is among the first three places in the country with the highest number of reported cases, the majority corresponding to the male sex. The key clinical characteristic is the sudden appearance of a focal neurological deficit. Imaging studies such as head computed tomography or magnetic resonance imaging allow us to differentiate the subtype and mechanism of CVD since treatment differs markedly between CVD of ischemic origin and that of hemorrhagic origin. Vitamin B12 or cobalamin is a tetrapyrrole cofactor; One of its functions is to participate in the metabolism of homocysteine, which has been reported in various studies and it has been shown that high levels of this increase the risk of vascular diseases, such as stroke. On the other hand, vitamin B12 deficiency can lead to platelet dysfunction, causing significant bleeding. There are few protocols that have sought the direct association of cobalamin with CVD and even fewer with the hemorrhagic type. This condition is one of the main causes of admission to the Emergency Service of the General Hospital of Mexicali where they are given the necessary attention such as performing imaging studies and taking laboratory samples and based on the results the treatment to be followed is decided; However, measurements of vitamin B12 levels are not performed in this population. If the association is demonstrated, it could be implemented as a preventive measure for cerebral vascular events.

Study Overview

Detailed Description

General objective: To demonstrate if there is a difference between serum levels of vitamin B12 in patients with hemorrhagic cerebral vascular event compared to patients with ischemic cerebral vascular event.

Specific objectives

  • Describe the characteristics of the study population (sex, age, comorbidities, laboratory diagnoses)
  • Determine serum levels of vitamin B12 in patients with cerebral vascular event
  • Establish the prevalence of vitamin B12 deficiency in patients with cerebral vascular events.
  • Correlations of vitamin B12 deficiency with the severity of the disease
  • To establish whether there is a difference in serum vitamin B12 levels between patients with ischemic stroke compared to hemorrhagic stroke.
  • Determine if the degree of deficiency correlates with mortality
  • Compare vitamin B12 levels by subgroups

STUDY DESIGN This will be a prospective, observational, analytical study of patients admitted to the General Hospital of Mexicali with a diagnosis of ischemic or hemorrhagic stroke.

SOURCE FOR OBTAINING PATIENTS Patients admitted to the adult emergency department of the Mexicali General Hospital with a diagnosis of ischemic or hemorrhagic stroke are included. The information will be collected from the electronic clinical record.

Non-probability sampling for convenience. Select all patients who arrive at the hospital who meet inclusion criteria and do not have any exclusion or elimination criteria.

Study Type

Observational

Enrollment (Estimated)

100

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

Study Locations

    • Baja California
      • Mexicali, Baja California, Mexico, 21000

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

No

Sampling Method

Probability Sample

Study Population

Select all patients who arrive at the hospital who meet inclusion criteria and do not have any exclusion or elimination criteria.

Description

Inclusion Criteria:

  • Age over 18 years
  • Have a diagnosis of a cerebral vascular event
  • Being a hospitalized patient at the General Hospital of Mexicali

Exclusion Criteria:

  • Patients without lab tests during their hospitalization
  • Patients without a cranial CT scan

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients with ischemic stroke
measure serum vitamin b12 levels
Measure the vitamin b-12 levels in patients that are admitted for stroke of any kind
patients with hemorrhagic stroke
measure serum vitamin b12 levels
Measure the vitamin b-12 levels in patients that are admitted for stroke of any kind

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference of vitamin B12 level between ischemic and hemorrhagic stroke
Time Frame: November 2023 - November 2024
Demonstrate if there is a difference between serum levels of vitamin B12 in patients with hemorrhagic cerebral vascular event compared to patients with ischemic cerebral vascular event.
November 2023 - November 2024

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vitamin B12 defficiency in patients with stroke
Time Frame: November 2023 - November 2024
Vitamin B12 defficiency in patients with any kind of stroke
November 2023 - November 2024
Population characteristics
Time Frame: November 2023 - November 2024
Determine if variables like sex, age, comorbilities and lab tests have a correlation between stroke and Vitamin B12 levels
November 2023 - November 2024
Mortality and vitamin B 12 deficiency in this specific population
Time Frame: November 2023 - November 2024
Analize the levels of vitamin B12 and the in-hospital mortality in this population
November 2023 - November 2024
Levels of B12 vitamin and severity of stroke
Time Frame: November 2023 - November 2024
Analize if there is a significant difference between the levels of B12 and the severity of stroke
November 2023 - November 2024

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

November 13, 2023

Primary Completion (Estimated)

July 1, 2024

Study Completion (Estimated)

November 30, 2024

Study Registration Dates

First Submitted

December 19, 2023

First Submitted That Met QC Criteria

December 19, 2023

First Posted (Actual)

January 5, 2024

Study Record Updates

Last Update Posted (Actual)

January 5, 2024

Last Update Submitted That Met QC Criteria

December 19, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

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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