Viewing Study NCT01967602


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Study NCT ID: NCT01967602
Status: UNKNOWN
Last Update Posted: 2013-10-23
First Post: 2013-10-18
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Biomarker of Lung Injury in ARDS Patients Receiving ECMO Support
Sponsor: National Taiwan University Hospital
Organization:

Study Overview

Official Title: Biomarker of Lung Injury in ARDS Patients Receiving ECMO Support
Status: UNKNOWN
Status Verified Date: 2013-10
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ARDS
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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: