Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID07291908

Correlation of Inflammation Severity With Pulmonary Gas Exchange and MiRNA-126 in Trauma Patients

Led by Melike Cengiz · Updated on 2025-12-18

130

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates the relationship between the severity of inflammation and lung function impairment in patients who have experienced trauma. It focuses on how markers of inflammation, such as C-reactive protein, procalcitonin, IL-6, and others, relate to lung injury risk and gas exchange problems. The study also explores the role of circulating microRNA-126 (miR-126) in maintaining lung barrier integrity and its potential in reflecting inflammatory burden after trauma. The study observes trauma patients admitted to intensive care units, including those who develop acute respiratory distress syndrome (ARDS) and those who do not, alongside a control group of healthy volunteers. Researchers collect blood samples, perform ultrasounds to assess vascular function, and measure clinical parameters like blood pressure and heart rate over the first three days of ICU admission. These assessments aim to correlate laboratory inflammation markers, imaging findings, and pulmonary gas-exchange measurements. Participants will be monitored closely for at least three days in intensive care, during which various blood tests, arterial blood gases, and ultrasound imaging are performed. The study measures the primary outcome as the correlation between serum miR-126 levels and lung injury severity in the initial ICU period. Secondary outcomes include levels of IL-6, syndecan, and flow-mediated dilation assessed by ultrasound. The findings may help identify biomarkers useful for predicting lung complications and guiding care after severe trauma.

CONDITIONS

Brief Title

Inflammation Severity and miRNA-126 in Trauma

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Patients monitored and treated for trauma in the anesthesia intensive care units
  • Patients who remain in intensive care for at least 3 days after trauma
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years
  • Patients with concomitant thoracic trauma
  • Presence of active infection prior to trauma
  • Patients not admitted to the ICU within the first 24 hours after trauma
  • Patients who remain in the ICU for less than 72 hours following trauma
  • Current use of steroids, chemotherapy, or antibiotic therapy prior to ICU admission
  • Patients with immunodeficiency
  • Patients who are in shock prior to or during ICU admission

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - At least 3 days after trauma

Participants who have experienced trauma are monitored in the intensive care unit to assess inflammation severity, pulmonary gas exchange, and circulating miR-126 levels.

Daily assessments during ICU stay for up to 3 days

Trial Site Locations

Total: 1 location

1

Akdeniz University Hospital

Antalya, Ağrı, Turkey (Türkiye), 04200

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Research Team

M

Melike Cengiz, Prof Dr

C

Canberk Kurban

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

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Frequently Asked Questions

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Published Research Related To This Trial

The Role of MicroRNAs in Acute Respiratory Distress Syndrome and Sepsis, From Targets to Therapies: A Narrative Review.

Lisa K Lee, Lejla Medzikovic, Mansoureh Eghbali...

https://pubmed.ncbi.nlm.nih.gov/33079870