Microcirculation and Oxidative Stress in Critical Ill Patients in Surgical Intensive Care Unit

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00808691
Collaborator
(none)
124
1
46
2.7

Study Details

Study Description

Brief Summary

As medicine advances, many lives can be saved in the intensive care unit. However, when multiple organ failure occurs, the mortality rate of patients increases dramatically. Therefore, the major goal in the intensive care unit is to prevent the occurrence of multiple organ failure. The sepsis protocol and early goal directed treatment have great effects to reduce development of multiple organ failure and to decrease the mortality rate. However, sometime the condition of patient deteriorated in spite of both the mean blood pressure and mixed venous oxygen saturation are normal. Some experts recognize that there might be microcirculatory dysfunction of tissue or organ. The dysfunction of microcirculation might due to vasoconstriction or microthrombosis. Vasoconstriction might result from systemic inflammation, reactive oxygen species, or dysfunction of synthesis of NO (nitric oxide). Microthrombosis might result from systemic inflammation, reactive oxygen species, imbalance of coagulatory system, or damage of endothelial cell.

In clinical practice, the oxidative stress is related to circulatory shock, sepsis, acute lung injury, and acute respiratory distress syndrome. This study tries to investigate the relation between oxidative stress and microcirculation. Furthermore, the investigators will try to investigate the correlation between the severity of oxidative stress and microcirculatory dysfunction and the severity of disease and prognosis. The investigators hope this study will help them to figure out the picture of disease progression of patients. It may conduct further study to modulate the oxidative stress, to improve the microcirculatory function, and finally to improve the outcome of patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Critical care

Study Design

Study Type:
Observational
Actual Enrollment :
124 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Microcirculation and Oxidative Stress in Critically Ill Patients in Surgical Intensive Care Unit
Study Start Date :
Sep 1, 2007
Actual Primary Completion Date :
Jul 1, 2010
Actual Study Completion Date :
Jul 1, 2011

Arms and Interventions

Arm Intervention/Treatment
1

Patients with sepsis

Other: Critical care
Standard care for each group of patients

2

Patient admitted for postoperative care

Other: Critical care
Standard care for each group of patients

3

Patients with ARDS

Other: Critical care
Standard care for each group of patients

4

Patients with ARF

Other: Critical care
Standard care for each group of patients

5

Patients who receive liver support treatment

Other: Critical care
Standard care for each group of patients

6

Patients wiht brain death

Other: Critical care
Standard care for each group of patients

Outcome Measures

Primary Outcome Measures

  1. Mortality Severity of Organ Failure [28 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 y/o

  • Related diagnosis made within 24h

  • Group 1 - Sepsis

  • Group 2 - Postoperative care

  • Group 3 - ARDS

  • Group 4 - Renal failure

  • Group 5 - Liver failure

  • Group 6 - Brain death

Exclusion Criteria:
  • Pregnant patients

  • Related diagnosis made longer than 24h

  • Patients who have received antioxidants within 24h

  • Patients who have received hyperbaric oxygen therapy

  • Patients who have a hemoglobin value less than 9 g/dl

  • Patients who have received NO

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital Taipei Taiwan

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Yu-Chang Yeh, M.D, National Taiwan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT00808691
Other Study ID Numbers:
  • 200707012
First Posted:
Dec 16, 2008
Last Update Posted:
Jan 6, 2015
Last Verified:
Jan 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 6, 2015