Evaluation of IL-33 in Patients With the Acute Ischemic Stroke

Sponsor
Jan Biziel University Hospital No 2 in Bydgoszcz (Other)
Overall Status
Unknown status
CT.gov ID
NCT03948802
Collaborator
(none)
90
1
24
3.7

Study Details

Study Description

Brief Summary

Aim of the study is to evaluate the usefulness of interleukin 33 in the blood plasma in patients with the acute ischemic stroke of the brain in relation to mode of treatment (thrombolysis, thrombectomy, no treatment), risk factors in correlation with other inflammatory state markers (hsCRP, morphology with smear ). Blood is collected on the first and seventh days of stroke.

The purpose is to clarify utility of IL 33 as a biomarker of acute stroke.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Interleukine 33 test in blood plasma

Detailed Description

Stroke is the third most frequent cause of death in highly developed countries (after heart disease and cancer), the main cause of disability in adults and the second most frequent cause of dementia syndromes. The annual incidence of stroke in the general population is approximately 0.2%. The risk of stroke increases with age.

Globally 15 million people are affected each year and 5.5 million die every year for this reason (20% in 30 days and up to 40% in a year from getting ill). In Poland, the incidence of stroke is around 175/100,000 in men and 125/100 in women.It is assumed that the cause of sudden cerebral insufficiency is mainly the embolism coming from the newly formed wall clot forming at the site of the atherosclerotic plaque rupture.

In recent years, the role of inflammatory factors is associated with the occurrence of severe atherosclerotic complications such as stroke or heart attack. Cytokines are glycoproteins that are released by activated cells of various tissues. They have a significant impact on the inflammation processes, they control all phases of the immune response. Interleukin is one of the cytokine groups. This study aims to find a relationship between level of IL 33 concentration and the size of the stroke and neurological deficit.

Blood will be collected on the first and seventh days of stroke for examination of Il 33, blood morphology and hsCRP

Study Design

Study Type:
Observational
Anticipated Enrollment :
90 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Evaluation of Interleukin 33 in Relation to Selected Inflammatory Parameters in Patients With the Acute Ischemic Stroke of the Brain
Actual Study Start Date :
Jan 1, 2019
Anticipated Primary Completion Date :
Jan 1, 2020
Anticipated Study Completion Date :
Jan 1, 2021

Arms and Interventions

Arm Intervention/Treatment
STROKE GROUP

Cerebral ischemic stroke patients treated.

Diagnostic Test: Interleukine 33 test in blood plasma
ELISA test for Interleukin 33

CONTROL GROUP

Ambulatory healthy patients

Diagnostic Test: Interleukine 33 test in blood plasma
ELISA test for Interleukin 33

Outcome Measures

Primary Outcome Measures

  1. NIHSS The National Institutes of Health Stroke Scale [7 days]

    Score 0-6 gently course of the cerebral stroke more than 6 increased manifestations of the cerebral infarction.Patients will be assessed before and after the trial to compare how each participant improved after given the intervention.

  2. DRAGON scale [7 days]

    Comparison of patients in DRAGON scale on the 1st and the 7th day. DRAGON scale was developed to make early predictions about clinical outcomes for ischemic stroke patients using only information that is available shortly after they arrive at the hospital and before tPA is given. The DRAGON score, especially at the low and high end of the scale, can help predict which patients are likely to have good clinical outcomes and those who are likely to have miserable clinical outcomes even if given tPA. These patients may also be potential candidates for endovascular thrombectomy, though the benefits of this procedure have not yet been demonstrated in the literature.

  3. ASTRAL scale [1 day]

    ASTRAL scale is used in patients with acute ischemic stroke admitted within 24 hours of stroke onset. It can provide additional information on medium-term functional outcome in patients that have suffered acute ischemic stroke, in addition to clinical judgment based on relevant clinical and laboratory variables.It can be used to adjust for functional outcome in multivariate models in acute stroke-related research studies.It can serve as a selection criterion for cohorts in acute stroke-related research studies.

  4. Modified Rankin Scale [7 days]

    Change in disability. mRS can help users determine the degree of disability in patients who have suffered a stroke. mRS assesses disability in patients who have suffered a stroke and is compared over time to check for recovery and degree of continued disability. A score of 0 is no disability, 5 is disability requiring constant care for all needs; 6 is death

  5. IL 33 and hsCRP concentration [7 days]

    Evaluation of IL 33 and hsCRP concentration, morphology with smear on the first and seventh day.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age over 18

  • Consent on participation

  • Diagnosed Ischemic Stroke

Exclusion Criteria:
  • Active cancer disease

  • Kidney failure

  • Liver failure

  • Pregnancy

  • Breastfeeding

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jan Biziel University Hospital nr 2 Collegium Medicum Nicolaus Copernicus University Bydgoszcz Poland 86-168

Sponsors and Collaborators

  • Jan Biziel University Hospital No 2 in Bydgoszcz

Investigators

  • Principal Investigator: PaweÅ‚ Sokal, Jan Biziel University Hospital Collegium Medicum Nicolaus Copernicus University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pawel Sokal, Head of Department of Neurosurgery and Neurology, Jan Biziel University Hospital No 2 in Bydgoszcz
ClinicalTrials.gov Identifier:
NCT03948802
Other Study ID Numbers:
  • JBUH-NN-STROKE-IL33
First Posted:
May 14, 2019
Last Update Posted:
Jun 3, 2019
Last Verified:
May 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pawel Sokal, Head of Department of Neurosurgery and Neurology, Jan Biziel University Hospital No 2 in Bydgoszcz
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 3, 2019