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Biomarker of Lung Injury in ARDS Patients Receiving ECMO Support

Biomarker of Lung Injury in ARDS Patients Receiving ECMO Support

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01967602
Acronym
ARDS
Enrollment
70
Registered
2013-10-23
Start date
2011-10-31
Completion date
2015-04-30
Last updated
2013-10-23

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

Conditions

ARDS, Multi-organ Failure

Keywords

Acute respiratory distress syndrome (ARDS), Extracorporeal membrane oxygenation (ECMO), biomarker

Brief summary

The goal of this project is to find a marker expression that the investigators can use to trace symptom progression and develop a more efficient therapy to enhance ARDS patient survival rate and better post-ICU life quality.

Detailed description

The investigators will first identify acute respiratory distress syndrome (ARDS) patients receiving ECMO support in ICU at National Taiwan University Hospital, and then collect blood, urine and bronchioalveolar lavage fluid (BALF) samples at different time points: before setting up ECMO, 2, 6, 12, 24, 72 hours,5 and 14 days after ECMO installment, time to wean ECMO and the day removing ECMO and leaving ICU. From the samples, the free radicals, cytokines (IL-1, IL-6, IL-8, IL-18,tumor necrosis factor-α, transforming growth factor-β), and inflammasome- related markers, immune cell responses and other biochemical markers would be measured. The novel biomarkers to predict the outcome of the patient will be identified.

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

1. \>18 years old 2. ARDS, needing ECMO support

Exclusion criteria

1. pre-existing sepsis 2. pre-existing chronic renal failure (dialysis dependent), liver failure other diseases precluding chance of survival.

Design outcomes

Primary

MeasureTime frameDescription
Mortality or multi-organ failure7 daysPatients who survived for more than 7 days after ECMO treatment were defined as survival, and non-survival patients were defined as expired or multiple organ failure incompatible with life within 7 days after ECMO installation.

Countries

Taiwan

Outcome results

None listed

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