Traumatic Endotheliopathy: A Prospective Observational Study of 424 Severely Injured Patients.
Pär I Johansson, Hanne H Henriksen, Jakob Stensballe...
https://pubmed.ncbi.nlm.nih.gov/27144442Actively Recruiting
Led by Melike Cengiz · Updated on 2025-12-18
130
Participants Needed
1
Research Sites
17 weeks
Total Duration
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
Inflammation Severity and miRNA-126 in Trauma
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Total: 1 location
1
Akdeniz University Hospital
Antalya, Ağrı, Turkey (Türkiye), 04200
Actively Recruiting
M
Melike Cengiz, Prof Dr
C
Canberk Kurban
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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Pär I Johansson, Hanne H Henriksen, Jakob Stensballe...
https://pubmed.ncbi.nlm.nih.gov/27144442Lisa K Lee, Lejla Medzikovic, Mansoureh Eghbali...
https://pubmed.ncbi.nlm.nih.gov/33079870