Actively Recruiting

Age: 18Years +
All Genders
ID06254313

The Role of CXCR4-expressing Neutrophils in Influenza-related Acute Respiratory Distress Syndrome

Led by University Hospital, Bordeaux · Updated on 2024-12-27

90

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Influenza remains a major global health threat, causing over 650,000 deaths annually without significant advances in patient care despite decades of research. Severe influenza can lead to acute lung injury due to a disrupted immune response, where neutrophils play a role in both fighting infection and disease tolerance. This study focuses on a specific subgroup of neutrophils that express CXCR4, which may be linked to worsening lung infections. Researchers aim to compare the levels of these CXCR4-expressing neutrophils in the blood and lung fluid of influenza patients who survive versus those who do not. Participants will undergo blood sampling and bronchoalveolar lavage (BAL) within 24 hours and again on day 3 after ICU admission to collect neutrophils. These cells will be isolated and analyzed through immunostaining and flow cytometry to measure the percentage of CXCR4-expressing neutrophils. Additionally, extra blood tubes and lung fluid samples will be collected during treatment for detailed study. The mortality rates of participants will be assessed at 28 and 90 days after inclusion. During the study, participants will be closely monitored with blood and lung fluid tests to evaluate immune cell behavior. Researchers will collect clinical data and mortality outcomes to understand the relationship between CXCR4-expressing neutrophils and disease severity. The study's findings aim to shed light on immune mechanisms in influenza-related acute respiratory distress syndrome and may help guide future therapies. Participant involvement will last at least 90 days, covering initial ICU admission through follow-up assessments.

CONDITIONS

Official Title

The Role of Cxcr4Hi neutrOPhils in InflueNza

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged 18 yo or above.
  • Acute respiratory distress syndrome as defined by the Berlin classification.
  • Invasive mechanical ventilation for less than 24 hours.
  • Cause of ARDS: Influenza infection proven by polymerase chain reaction OR Bacterial infection (tracheal aspirate with more than 105 CFU/mL and BAL with more than 104 CFU/mL) OR Pancreatitis according to the 2013 Working Group IAP/APA Acute Pancreatitis Guidelines OR Peritonitis according to the 2018 SFAR guidelines.
  • Health insurance.
  • Written informed consent from legal relative or representative.
Not Eligible

You will not qualify if you...

  • Neutropenia (< 500/mm3).
  • Neutrophils qualitative defect.
  • Patient included in an interventional research assessing an immunomodulatory or antiviral drug.
  • Acquired ImmunoDeficiency Syndrome.
  • Contraindication to BAL: Severe bronshospasm, Out-of-control shock, Intracranial high pressure, Refractory hypoxemia (PaO2/FiO2 < 60 mmHg).
  • Legal restriction: prisoners, pregnancy, legal protection.

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Hopital Pellegrin

Bordeaux, France, 33000

Actively Recruiting

2

Hopital Haut-Lévêque

Pessac, France, 33604

Not Yet Recruiting

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Research Team

R

Renaud PREVEL, Dr

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

Frequently Asked Questions

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The Role of CXCR4-expressing Neutrophils in Influenza-related Acute Respiratory Distress Syndrome | DecenTrialz