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Serial Changes of Soluble Triggering Receptor Expressed on Myeloid Cells-1 (sTREM-1) Levels in Patients With Acute Respiratory Distress Syndrome

Serial Changes of sTREM-1 Levels in Patients With Acute Respiratory Distress Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00557414
Enrollment
63
Registered
2007-11-14
Start date
2007-10-31
Completion date
2008-03-31
Last updated
2008-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

Keywords

acute respiratory distress syndrome, soluble triggering receptor expressed on myeloid cells-1, prognosis

Brief summary

The purpose of this study is to determine the impact of the serum soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) on etiology and prognosis of acute respiratory distress syndrome (ARDS)

Detailed description

The triggering receptor expressed on myeloid cells-1 (TREM-1), a member of the immunoglobulin superfamily, is upregulated on phagocytic cells in the presence of bacteria or fungi infection and weakly expressed in samples from patients with noninfectious inflammatory disorders. In addition, TREM-1 is shed from the membrane of activated phagocytes and can be found in a soluble form (sTREM-1) in body fluids. The level and serial change of a serum sTREM-1 from cirtical ill patients has been shown to be a good diagnostic and prognostic indicator of ventilation associated pneumonia (VAP) and severe sepsis.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Fulfill clinical diagnosis of ARDS * Require mechanical ventilation support

Exclusion criteria

* Pregnant * Immunocompromised

Design outcomes

Primary

MeasureTime frame
all cause mortality28 days
Septic or non-septic etiologyAt enrollment

Secondary

MeasureTime frame
CRP, lactate, WBC count, APACHE II score, LIS, SOFA scoreAt enrollment
IL-1 beta, IL-8, TNF-alphaserial follow up at Day 1, 3, 5, 7, 14

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026