Copeptin: Disease Severity Indicator

Last updated: May 28, 2024
Sponsor: Berker Okay
Overall Status: Completed

Phase

N/A

Condition

Bronchitis

Pneumonia (Pediatric)

Pneumonia

Treatment

Copeptin level measurement

Clinical Study ID

NCT06211985
63-2023
  • Ages 1-5
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Copeptin serves as a biomarker emanating from the pituitary gland, functioning as the precursor to arginine vasopressin (AVP). Its role in the regulation of endothelial dysfunction, inflammation, and water-electrolyte balance has been established. The measurement of AVP levels poses challenges due to its brief half-life and the intricate nature of its detection method. In contrast, copeptin provides an indirect means of gauging circulating AVP levels, as it can be conveniently assessed through a sandwich immunoassay. As a neuroendocrine stress hormone, copeptin emerges as a prognostic indicator, reflective of an individual's stress burden. Moreover, its applicability extends to various acute conditions such as ischemic stroke or myocardial infarction. Notably, copeptin proves to be a dependable tool in the differential diagnosis of diverse ailments characterized by polyuria and polydipsia.

Lower respiratory tract infection (LRTI) stands as the predominant cause of morbidity and mortality among children and adolescents globally. Notably, copeptin has demonstrated utility in forecasting the severity and complications associated with severe pneumonia in adults. While early investigations into copeptin's role in pediatric LRTI suggest its potential for diagnosing pneumonia and predicting complications, the outcomes of these studies present conflicting results.

Although there has been a notable increase in studies on copeptin in pediatric patients over the past decade, research specifically exploring its correlation with pneumonia remains scarce. This prospective case-control study is designed to investigate the potential association between copeptin levels and the severity of illness in pediatric patients with pneumonia. The study aims to determine whether copeptin levels can serve as a reliable predictor of disease severity in pneumonia, offering valuable insights for clinical application. The outcomes of this research may contribute significantly to our comprehension of copeptin's role in disease prognosis and management, thereby facilitating the development of more efficacious diagnostic and therapeutic approaches. Additionally, the study seeks to identify the factors influencing copeptin levels and establish a cut-off value for copeptin in pediatric patients diagnosed with pneumonia.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Being diagnosed with pneumonia,

  • The family must have given informed consent for the study.

Exclusion

Exclusion Criteria:

  • Individuals with underlying lung conditions (such as cystic fibrosis,bronchopulmonary dysplasia, asthma, bronchiectasis, tuberculosis),

  • Individuals with underlying chronic illnesses (inclusive of heart, kidney, liver,gastrointestinal, and endocrine disorders),

  • Individuals with obesity or malnutrition,

  • Individuals with hyponatremia detected in their tests,

  • Individuals with signs of dehydration,

  • Individuals with a history of hospitalization within the last 72 hours.

Study Design

Total Participants: 101
Treatment Group(s): 1
Primary Treatment: Copeptin level measurement
Phase:
Study Start date:
April 12, 2023
Estimated Completion Date:
November 02, 2023

Connect with a study center

  • UHS Haseki Training and Research Hospital

    Istanbul, Sultangazi 34304
    Turkey

    Site Not Available

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