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Completed

NCT Number: NCT03594695

Hs-CRP and NLR as Markers of Perioperative Stress

The stress response to surgery is a result of tissue injury with local and systemic inflammation that contributes to the postoperative outcome. Anesthesia is known to effect perioperative stress response Regional anesthesia modifies stress response through afferent blockage whereas general anesthesia affects the stress response via central modulation. High sensitive C-reactive protein and neutrophil to lymphocyte ratio are used for evaluation of inflammation. The aim of this study was to document the value hs-CRP and NLR in perioperative stress response in two different anesthesia methods applied to term pregnant women undergoing elective ceserean section (C/S).

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Key information

Age range

18 year–42 year

Sex eligibility

Female

Study type

Observational

Primary location

Ufuk University

Ankara, Balgat, 06520, Turkey (Türkiye)

About this study

The stress response to surgery is a result of tissue injury with local and systemic inflammation that contributes to the postoperative outcome. Anesthesia is known to effect perioperative stress response. Regional anesthesia modifies stress response through afferent blockage whereas general anesthesia affects the stress response via central modulation. High sensitive C-reactive protein and neutrophil to lymphocyte ratio are used for evaluation of inflammation. The degree of systemic inflammation has been determined by numerous pro- and anti-inflammatory cytokines.The cytokines control the release of C -reactive protein (CRP) which is an acute phase reactant produced by the liver. CRP is a widely used marker of inflammation and tissue damage. High sensitive C -reactive protein (hs-CRP), is a more sensitive assay for detection of inflammation measured by particle-enhanced immunonephelometry . A rapid increase in hs-CRP may indicate inflammation and tissue damage . Another well-known indicator of inflammation is neutrophil-to-lymphocyte ratio (NLR). NLR correlates strongly with elevated plasma levels of circulating proinflammatory cytokineS. The aim of this study was to document the value hs-CRP and NLR in perioperative stress response in two different anesthesia methods applied to term pregnant women undergoing elective ceserean section (C/S).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Healthy pregnant women without chronic diseases at term (36-41 weeks of pregnancy)

Exclusion criteria

  • refusal to participate,
  • chronic diseases (diabetes mellitus, hypertension, heart disease, renal disease, hypo/hyperthyroidism)
  • any infections,
  • smoking
  • contraindications for central neuraxial anesthesia.
  • Pregnancies complicated with rupture of membranes, placenta previa, eclampsia/preeclampsia, and abruptio placenta
  • fetal anomalies,
  • abnormality detected at fetal well-being tests

Treatment and study plan

HSCRP and NLR

Diagnostic Test

hs-CRP levels and NLR values will be studied from routine blood samples.

Primary outcomes

  1. Evaluation of the change in HSCRP levels

    Time frame: preoperative, postoperative 2nd and 4th hours, fetal cord blood sample (following delivery)

    Measurement of high sensitive C reactive protein levels in different time points in order to evaluate the change in HSCRP levels

  2. Evaluation of the change in NLR

    Time frame: preoperative, postoperative 2nd and 4th hours, fetal cord blood sample (following delivery)

    Measurement of the Neutrophil to Lymphocyte Ratio in different time points in order to evaluate the change in the Neutrophil to Lymphocyte Ratios

Sponsors and collaborators

Lead sponsor

Ufuk University

Other

Registry information

Official study title

Hs-CRP and NLR as Markers of Perioperative Stress in Maternal And Fetal Blood in Different Anesthesia Techniques

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jul 20, 2018
Registry last updated
Oct 15, 2018

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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