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Completed

NCT Number: NCT04250935

Brain-Induced Neurotrophic Factor Levels in Patients Undergoing Coronary Artery Bypass Surgery

In patients undergoing coronary artery bypass surgery, the relationship between neurocognitive changes seen in the early period and brain-induced neurotrophic factor serum levels will be investigated.

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Key information

Age range

40 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Bozok University Medical Center

Yozgat, Turkey (Türkiye)

About this study

Although postoperative cognitive dysfunction (POKD) is the most common neurological complication in patients undergoing coronary artery bypass grafting (CABG) surgery, its pathophysiology is still not fully understood. However, the quality of this dysfunction has not been properly measured. In addition to clinical tests, biomarkers are often used to detect the presence of POKD. In this study, it was aimed to evaluate the relationship between intraoperative and postoperative brain-derived neurotrophic factor serum levels and POKD in patients undergoing CABG surgery.

This prospective observational study is planned to include 30 adult patients aged 40-90 years. Patients with stroke history, neurodegenerative disease, seizure history, alcohol use, general anxiety, hearing deficit, unilateral carotid artery stenosis greater than 70%, and carotid artery bilateral stenosis greater than 50% will be excluded from the study.

This study aimed to determine perioperative changes in serum brain-derived neurotrophic factor levels in patients undergoing CABG surgery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At Least Primary School Graduates,
  • Not Using Drugs That May Affect Cognitive Functions,
  • No Alcohol Substance Use,
  • Without Psychiatric And Neurological Diseases

Exclusion criteria

  • Uneducated Patients,
  • Drug Users Who May Affect Cognitive Functions (Antipsychotic, Antidepressant),
  • Have Alcohol And Substance Use Disorders,
  • Those With A History Of Central Nervous System Disease That May Cause Cognitive Dysfunction (Such As Stroke, Neurodegenerative Disease, Seizure, General Anxiety),
  • Hearing Deficit,
  • Patients With Unilateral Carotid Artery Stenosis Greater Than 70% And Bilateral Stenosis Greater than 50% Carotid Artery

Treatment and study plan

Patients with cognitive dysfunction

Diagnostic Test

Mini Mental Test Those with a score below 21 points

Primary outcomes

  1. Postoperative cognitive dysfunction

    Time frame: 4 days

    Relationship between serum brain-derived neurotrophic factor level and cognitive dysfunction

Sponsors and collaborators

Lead sponsor

Bozok University

Other

Registry information

Official study title

The Relationship Between Neurocognitive Changes and Brain-Induced Neurotrophic Factor Levels in Patients Undergoing Coronary Artery Bypass Surgery

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jan 31, 2020
Registry last updated
Dec 3, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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