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Oxidative Stress in Critical Ill Patients in Surgical Intensive Care Unit
This study is currently recruiting participants.
Verified by National Taiwan University Hospital, August 2009
First Received: September 2, 2008   Last Updated: September 4, 2009   History of Changes
Sponsored by: National Taiwan University Hospital
Information provided by: National Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT00745888
  Purpose

In clinical practice, the oxidative stress is related to circulatory shock, sepsis, acute lung injury, and acute respiratory distress syndrome. There are some questions on the oxidative stress of the critical illness. First, the investigators want to search out the effects of the past history, smoking, alcohol drinking, use of antioxidants, different diseases, and different duration of SIRS on the degree of oxidative stress. Second, besides total count of ROS, the investigators used new techniques to determine superoxide(O2●-), hydrogen peroxide (H2O2), and hypochlorous acid(HOCl). Furthermore, we want to investigate the correlation of the degree of different reactive oxygen species and the severity of SIRS or shock. Third, we try to investigate the correlation between the change of oxidative stress and the prognosis of the patients.

The investigators wish this study will help them to investigate the effect of oxidative stress on critical ill patients, to modulate the oxidative stress, to decrease the occurrence of SIRS, shock, and multiorgan failure, and to improve the long term outcome of patients.


Condition Intervention Phase
Sepsis
Shock
Other: Chemiluminescence Analyzer
Phase III

Study Type: Observational
Study Design: Prospective
Official Title: Oxidative Stress in Critical Ill Patients in Surgical Intensive Care Unit

Resource links provided by NLM:


Further study details as provided by National Taiwan University Hospital:

Primary Outcome Measures:
  • 28-day Survival [ Time Frame: 28 days ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Days stay in ICU Days on ventilator SOFA score Complications [ Time Frame: 28 days ] [ Designated as safety issue: No ]

Biospecimen Retention:   Samples Without DNA

Biospecimen Description:

blood sample


Estimated Enrollment: 200
Study Start Date: May 2007
Groups/Cohorts Assigned Interventions
1
age > 18 y/o Patients admitted to surgical ICU
Other: Chemiluminescence Analyzer
measure reactive oxygen species

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients admitted to surgical ICU

Criteria

Inclusion Criteria:

  • Age > 18 y/o
  • Admitted to surgical ICU

Exclusion Criteria:

  • Patients with brain death
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00745888

Contacts
Contact: Yu-Chang Yeh, MD 886-9-68661829 tonyyeh@ntuh.gov.tw

Locations
Taiwan
National Taiwan University Hospital Recruiting
Taipei, Taiwan, 100
Contact: Yu-Chang Yeh, MD     886-9-68661829     tonyyeh@ntuh.gov.tw    
Principal Investigator: Yu-Chang Yeh, MD            
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Yu-Chang Yeh National Taiwan University Hospital
  More Information

No publications provided

Responsible Party: National Taiwan University Hospital ( Yu-Chang Yeh )
Study ID Numbers: 9561709132
Study First Received: September 2, 2008
Last Updated: September 4, 2009
ClinicalTrials.gov Identifier: NCT00745888     History of Changes
Health Authority: Taiwan: Department of Health

Keywords provided by National Taiwan University Hospital:
oxidative stress
intensive care
Postoperative intensive care

Study placed in the following topic categories:
Sepsis
Shock
Stress

ClinicalTrials.gov processed this record on September 10, 2009