Inflammation and Post-Stroke Depression

Completed

Conditions studied: Stroke, Acute Stroke

In brief

This study is being done to see if there is a relationship between stroke, post-stroke depression, and measures of inflammatory and/or stress compounds in the blood. Brain injury, as caused by stroke, leads to an inflammatory response in the brain which in turn can influence inflammatory and stress responses in other parts of the body outside of the brain. These responses can be measured by analyzing various substances in the blood and in the white blood cells. The investigators will measure these substances (cytokines, glucocorticoids) and compare them to the absence, presence, or degree of depression that the investigators will determine by neurological and psychological testing. The investigators will be drawing blood for this study on admission, at or around day 3, at or around day 7 and at or around day 90, which is not part of routine stroke care. The investigators will be asking subjects to participate in answering question/scales on these same days, some of these questionnaires are also not part of routine stroke care. Standard stroke care is being done other than blood drawing/participating in answering questions/scales. Approximately 25 people will be enrolled over one year.

Key facts

Study ID

NCT02368145

Run by

Alexander Kusnecov, Ph.D.

People needed

25

Starts

2013-07-01

Expected to finish

2016-06-01

Last updated by the study team

2026-07-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The subjects will be male and female patients with acute ischemic stroke of the brain. Vascular risk factors, including diabetes, hypertension, and coronary artery disease, are expected to be common, and will be recorded in the Source Documents (appendix). Patients will be included if:
• Aged ≥ 18 years of age
• Neuroimaging or clinical symptoms are consistent with an acute ischemic stroke (AIS)
• There are no alternative explanations for symptoms (eg. tumor, witnessed seizure, history of complicated migraine headache, hypoglycemia [blood sugar (BS) < 50 mg/dL] or hyperglycemia (BS > 400 mg/dL)
• Subject is able to be enrolled and have blood samples drawn (Note: inability to provide a sample within 48 hours does not preclude inclusion if consent is provided after this time and patient can provide blood at subsequent time points (see Table)
• Subject is able to provide informed consent for participation in this research study

You may not qualify if…

• • Other known severe/terminal illness which limits life expectancy to < 90 days, sepsis, disseminated intravascular coagulopathy (DIC), infective endocarditis, metastatic cancer, or cerebral vasculitis
• Current diagnosis of or treatment for major depressive disorder
• Women who are pregnant at the time of stroke, since pregnancy alters inflammatory markers
• Communication problems due to aphasia at visit 2, inability to speak English
• History of substance abuse and other relevant psychiatric conditions
• Autoimmune, current or recent infection, hematological disorders, use of immune modulating drugs

Where it is running

• Rutgers, The State University — New Brunswick, New Jersey, United States

Full record on ClinicalTrials.gov

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