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OpenTrials
Completed

NCT Number: NCT00825357

Biological Markers to Identify Early Sepsis and Acute Lung Injury

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Intensive Care Medicine; Chi Mei Medical Center

Tainan, Taiwan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. The present study will focus on testing 'biological markers' to identify patients with sepsis and acute lung injury in early stage.

    Time frame: 72 hrs

Sponsors and collaborators

Lead sponsor

Chimei Medical Center

Other

Registry information

Important dates

Study start
2006
Primary completion
2011
Study completion
2011
First posted
Jan 21, 2009
Registry last updated
Jan 28, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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