Biological Markers to Identify Early Sepsis and Acute Lung Injury

NCT ID: NCT00825357

Last Updated: 2016-01-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-09-30

Study Completion Date

2011-08-31

Brief Summary

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There are no clear markers to identify sepsis and acute lung injury at early stage in clinical settings which would result in improved survival of the patients. In collaboration with the research team led by Dr. Zhang at St. Michael's Hospital, Toronto, we have initiated a pilot study looking for biological markers to detect severe sepsis and ARDS. We have found that human neutrophils peptides (a-defensins), certain coagulation variables and cytokine levels are very sensitive markers to differentiate severe sepsis, ARDS from cardiovascular diseases in ICU patients. These findings may provide valuable information for therapeutic guideline in clinical practice. The present study will focus on testing 'biological markers' to identify patients with sepsis and acute lung injury. We will examine the roles of three components of markers including inflammation, neutrophil activation and coagulation. We are hoping that this proposed translational research will help develop novel therapeutic strategy in sepsis and acute lung injury patients.

Detailed Description

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Conditions

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Sepsis Acute Lung Injury

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Meet diagnostic criteria of ≧2 SIRS or acute lung injury.
* Get agreement of patient's attending physician and inform consent form patient or family.

Exclusion Criteria

* Use Antibiotics over 24 hrs(only SIRS group).
* Active bleeding.
* Pregnancy.
* Active Cancer (refer to malignancy which is recently diagnosed, under treatment, or relapsed)
* VS or Subject or Family refuse
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Chimei Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Kuo-Chen Cheng

Chief

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department of Intensive Care Medicine; Chi Mei Medical Center

Tainan City, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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CM-IRB09509002

Identifier Type: -

Identifier Source: org_study_id

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