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Diagnostic and Prognostic Value of Combination Biomarkers in the Critically Ill Patient With Sepsis.

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified August 2012 by Jianfeng Xie, Southeast University, China.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01687010
First Posted: September 18, 2012
Last Update Posted: September 18, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Southeast University, China
Information provided by (Responsible Party):
Jianfeng Xie, Southeast University, China
  Purpose
Sepsis is a common cause for morbidity and mortality in critically ill patients. With the development of medical skills, the mortality is still remain very high. Inappropriateness of initial antibiotic treatment is an important risk factor for mortality and effective antimicrobial administration within the first hour of documented hypotension was associated with increased survival to hospital discharge in adult patients with septic shock. However, the early treatment based on early diagnosis.But it is very difficult to diagnosis because of lack of specific clinic symptom and sign.When severe sepsis occur, biomarker could be helpful to diagnosis. Unfortunately, the diagnostic value of single biomarker is limited. Therefore, combine several biomarkers could enhance the diagnostic value.

Condition
Diagnostic and Predictive Value

Study Type: Observational
Study Design: Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Jianfeng Xie, Southeast University, China:

Estimated Enrollment: 300
Study Start Date: March 2012
Estimated Study Completion Date: October 2012
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Critically ill patients
Criteria

Inclusion Criteria:

  • Critically ill patients admitted into ICU

Exclusion Criteria:

  • Age younger than 18 years
  • Refuse to participate in this study
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01687010


Contacts
Contact: Jianfeng Xie, M.D. +8602583272201 seuicu@yahoo.com.cn

Locations
China, Jiangsu
Department of Critical Care Medicine Nanjing Zhong-da Hospital Southeast University School of Medicine Recruiting
Nanjing, Jiangsu, China, 210009
Contact: Yi Yang, M.D., Ph.D,    +8602583272202    yiyiyang2004@yahoo.com.cn   
Sponsors and Collaborators
Jianfeng Xie
Southeast University, China
  More Information

Responsible Party: Jianfeng Xie, Physician of critical care department, Southeast University, China
ClinicalTrials.gov Identifier: NCT01687010     History of Changes
Other Study ID Numbers: PCT001
First Submitted: September 13, 2012
First Posted: September 18, 2012
Last Update Posted: September 18, 2012
Last Verified: August 2012

Keywords provided by Jianfeng Xie, Southeast University, China:
CRP, PCT, IL-6, Diagnosis, Prediction


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