Status:

COMPLETED

Relation Between Insulinoresistance and Neutrophile to Lymphocyte Ratio in Cardiac Surgery.

Lead Sponsor:

Centre Hospitalier Universitaire de Besancon

Conditions:

Insulin Resistance

Cardiac Surgery Requiring Cardiopulmonary Bypass

Eligibility:

All Genders

18+ years

Brief Summary

The University Hospital of Besançon is conducting a public interest research project called CRYSTAL, who studies the relationship between the Neutrophil to Lymphocyte ratio (NLR) and insulin resistanc...

Detailed Description

Coronary artery bypass graft (CABG) and heart valve replacement surgeries under cardiopulmonary bypass (CPB) are considered high-risk procedures, associated with a morbidity of 14% and a mortality rat...

Eligibility Criteria

Inclusion

  • Men and women aged over 18
  • Scheduled cardiac surgery
  • Blood count the day of admission to the IS
  • Subject not objecting to the use of their personal data and/or biological samples
  • Affiliation to a French social security scheme or beneficiary of such a scheme

Exclusion

  • Immunosuppressive treatment
  • Pre-existing corticosteroid therapy
  • Hematological pathologies
  • Current infection (current antibiotic therapy)
  • Active tumor disease
  • End-stage renal failure (DFG \< 30 ml/min/1.73m² or on dialysis)
  • Severe liver failure (TP \< 50%)
  • Diabetics on insulin
  • Admission to a care unit other than Thoracic and Cardiovascular Surgery Intensive Care (SI CTCV) in the immediate post-operative period
  • Pregnant women, parturients and breastfeeding mothers
  • Persons deprived of their liberty by a judicial or administrative decision; persons subject to psychiatric care under constraint; persons admitted to a health or social establishment for purposes other than research
  • Minors
  • Adults subject to a legal protection measure or unable to express their consent
  • Subject without health insurance
  • Subject in the exclusion period of another study or provided for by the "national volunteer file"

Key Trial Info

Start Date :

August 25 2024

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 18 2024

Estimated Enrollment :

211 Patients enrolled

Trial Details

Trial ID

NCT06945536

Start Date

August 25 2024

End Date

November 18 2024

Last Update

April 25 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

CHU Besançon

Besançon, France, 25000