Effect of Midazolam on Inflammatory Response and Organ Function in Mechanically Ventilated Sepsis Patients With Different Immune Status
Primary Purpose
Inflammatory Disorder of Immune System, Sepsis
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
blood sample collection
Midazolam
Morphine
Sedation interruption
Sponsored by
About this trial
This is an interventional treatment trial for Inflammatory Disorder of Immune System focused on measuring organ function, sedation
Eligibility Criteria
Inclusion Criteria:
- Mechanically ventilated ICU patients, sedation is needed.
- Sepsis patients.
- Age 18-80 yrs
- Anticipated sedation duration is more than 3 days.
- Agreed to participate the study and assigned the informed consent. -
Exclusion Criteria:
- Allergic to the Benzodiazepine.
- Hepatic dysfunction(Child-Pugh is C level).
- Participated other study.
- Bad prognosis and possibly become the major reason of patients death, such as sever craniocerebral injury,cardiopulmonary resuscitation,advanced malignant tumor,etc.
- History of immune system disease, immune treatment (including hormone ) or treatment that could affect immune function (including continuous renal replacement therapy,CRRT).
- Alcoholic and drug abuse.
- Tendency for major mental disease or treatment of anti psychotics.
- Pregnant,lactation woman.
- Unwilling to assign the informed consent or bad compliance. -
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
Normal immune function
Moderate immunosuppression
Sever immunosuppression
Immune paralysis
Arm Description
The value of monocyte human leukocyte antigen-DR (mHLA-DR) is equal to or more than 15000 monoclonal antibody.
The value of mHLA-DR is equal to or more than 10000 and less than 15000 monoclonal antibody.
The value of mHLA-DR is equal to or more than 5000 and less than 10000 monoclonal antibody.
The value of mHLA-DR is less than 5000 monoclonal antibody.
Outcomes
Primary Outcome Measures
T cell subset T Helper 1
T Helper 1(TH1) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
T cell subset T Helper 2
T Helper 2(TH2) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
T cell subset Regulatory T Cell
Regulatory T Cell are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
Interleukin-6
Levels of interleukin-6(IL-6) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Interleukin-10
Levels of interleukin-10(IL-10) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Tumo necrosis factor-α(TNF-α)
Levels of Tumo necrosis factor-α(TNF-α) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Secondary Outcome Measures
duration of mechanical ventilation
Number of Participants with Serious and Non-Serious Adverse Events
Mortality
Participants' mortality of 28 and 90 days is recorded, including state of survival, the date and the reason of death.
Length of ICU stay
Index of renal function
level of Blood Urea Nitrogen(BUN) and Creatinine(Cr).
Index of myocardial enzyme
level of Brain Natriuretic Peptide(BNP).
Index of hepatic function
level of glutamic-pyruvic transaminase(ALT),glutamic oxalacetic transaminase(AST),Total Bilirubin(Tbil).
Index of endocrine function
level of cortisol and blood glucose.
C-reaction protein
C-reaction protein(CRP)is tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Full Information
NCT ID
NCT02135055
First Posted
April 29, 2014
Last Updated
May 7, 2014
Sponsor
Xiangya Hospital of Central South University
1. Study Identification
Unique Protocol Identification Number
NCT02135055
Brief Title
Effect of Midazolam on Inflammatory Response and Organ Function in Mechanically Ventilated Sepsis Patients With Different Immune Status
Official Title
Effect of Midazolam on Inflammatory Response and Organ Function in Mechanically Ventilated Sepsis Patients With Different Immune Status.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2014 (undefined)
Primary Completion Date
March 2015 (Anticipated)
Study Completion Date
March 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xiangya Hospital of Central South University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
ICU patients always experience all kinds of pain, discomfort and sleep disturbance,especially the sepsis patients. Appropriate sedation and analgesia is must,the newest sepsis guideline strongly recommend that mechanically ventilated sepsis patients need sedation therapy.
Recent studies show than immune dysfunction dose have an important effect on the occurrence and development of sepsis. When the body suffer from the pathogenic microorganism attacking and sepsis, it activate the systemic inflammatory response (SIRS) and compensatory anti-inflammatory response syndrome (CARS). When it is out of balance between SIRS and CARS, the inflammatory response, immune paralysis or immune dysfunction occurs and the mixed anti-inflammatory response syndrome (MARS) exists, and then the multiple organ dysfunction. So, immune dysfunction is thought to be the key factors on the development of the sepsis. Some studies show that the sedation drug such as midazolam, propofol, dexmedetomidine could suppress the inflammatory response effectively and then modulate the immune function.
Several recent studies show that midazolam has the immunoregulation effect and trend of suppress the inflammatory response, but the result is controversy, the possibly reason is the different immune status. Now there is the guideline about the different immune status: the normal immune function means that the value of mHLA-DR is more than 15000 monoclonal antibody; moderate-sever immune suppression means that the value of mHLA-DR is in the range of 5000 and 15000 monoclonal antibody; the immune paralysis means that the value of mHLA-DR is less than 5000 monoclonal antibody.
The purpose of the study is to explore the effect of midazolam to inflammatory response and organ function at mechanically ventilated sepsis patients who have different immune status.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Disorder of Immune System, Sepsis
Keywords
organ function, sedation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Normal immune function
Arm Type
Experimental
Arm Description
The value of monocyte human leukocyte antigen-DR (mHLA-DR) is equal to or more than 15000 monoclonal antibody.
Arm Title
Moderate immunosuppression
Arm Type
Experimental
Arm Description
The value of mHLA-DR is equal to or more than 10000 and less than 15000 monoclonal antibody.
Arm Title
Sever immunosuppression
Arm Type
Experimental
Arm Description
The value of mHLA-DR is equal to or more than 5000 and less than 10000 monoclonal antibody.
Arm Title
Immune paralysis
Arm Type
Experimental
Arm Description
The value of mHLA-DR is less than 5000 monoclonal antibody.
Intervention Type
Other
Intervention Name(s)
blood sample collection
Intervention Description
Patients were included 1 hrs later(before the study drug is administrated), 3 d and 7 d after sedation with midazolam, blood sample is collected. Flow cytometry is performed to test the mHLA-DR and according the value of mHLA-DR, assign the participant to the 4 groups as described in the arm.
Intervention Type
Drug
Intervention Name(s)
Midazolam
Other Intervention Name(s)
Liyuexi
Intervention Description
The loading dose of midazolam is 0.03-0.3 mg/kg, intravenous injected slowly for 10 minutes, then 0.04-0.2 mg/kg/h for maintenance of sedation.
Intervention Type
Drug
Intervention Name(s)
Morphine
Intervention Description
Morphine is the only analgesic drug that permitted to use. 2 mg morphine is given a bolus when the participant feel pain. If the pain is not alleviated, 0.4-1 mg/h morphine is maintained.
Intervention Type
Procedure
Intervention Name(s)
Sedation interruption
Intervention Description
Sedation interruption is performed at 8 am every morning.
Primary Outcome Measure Information:
Title
T cell subset T Helper 1
Description
T Helper 1(TH1) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
Time Frame
Change from baseline of T Helper 1 at 3 and 7 days.
Title
T cell subset T Helper 2
Description
T Helper 2(TH2) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
Time Frame
Change from baseline of T Helper 2 at 3 and 7 days.
Title
T cell subset Regulatory T Cell
Description
Regulatory T Cell are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
Time Frame
Change from baseline of Regulatory T Cell at 3 and 7 days.
Title
Interleukin-6
Description
Levels of interleukin-6(IL-6) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Time Frame
Change from baseline of Interleukin-6 at 3 and 7 days.
Title
Interleukin-10
Description
Levels of interleukin-10(IL-10) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Time Frame
Change from baseline of Interleukin-10 at 3 and 7 days.
Title
Tumo necrosis factor-α(TNF-α)
Description
Levels of Tumo necrosis factor-α(TNF-α) are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Time Frame
Change from baseline of TNF-α at 3 and 7 days.
Secondary Outcome Measure Information:
Title
duration of mechanical ventilation
Time Frame
from the begining of ventilation to weaning, up to 7 days.
Title
Number of Participants with Serious and Non-Serious Adverse Events
Time Frame
up to 7 days
Title
Mortality
Description
Participants' mortality of 28 and 90 days is recorded, including state of survival, the date and the reason of death.
Time Frame
up to 28 days
Title
Length of ICU stay
Time Frame
from ICU admmittion to discharge from ICU,up to 28 days.
Title
Index of renal function
Description
level of Blood Urea Nitrogen(BUN) and Creatinine(Cr).
Time Frame
baseline,the 3rd and 7th day after sedation
Title
Index of myocardial enzyme
Description
level of Brain Natriuretic Peptide(BNP).
Time Frame
baseline,the 3rd and 7th day after sedation
Title
Index of hepatic function
Description
level of glutamic-pyruvic transaminase(ALT),glutamic oxalacetic transaminase(AST),Total Bilirubin(Tbil).
Time Frame
baseline,the 3rd and 7th day after sedation
Title
Index of endocrine function
Description
level of cortisol and blood glucose.
Time Frame
baseline,the 3rd and 7th day after sedation
Title
C-reaction protein
Description
C-reaction protein(CRP)is tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Enzyme Linked Immunosorbent Assay(ELISA).
Time Frame
baseline,the 3rd and 7th day after sedation
Other Pre-specified Outcome Measures:
Title
mHLA-DR
Description
Levels of mHLA-DR are tested before sedation, 3 d and 7 d after sedation with midazolam.
The test method is Flow cytometry.
Time Frame
baseline,the 3rd and 7th day after sedation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mechanically ventilated ICU patients, sedation is needed.
Sepsis patients.
Age 18-80 yrs
Anticipated sedation duration is more than 3 days.
Agreed to participate the study and assigned the informed consent. -
Exclusion Criteria:
Allergic to the Benzodiazepine.
Hepatic dysfunction(Child-Pugh is C level).
Participated other study.
Bad prognosis and possibly become the major reason of patients death, such as sever craniocerebral injury,cardiopulmonary resuscitation,advanced malignant tumor,etc.
History of immune system disease, immune treatment (including hormone ) or treatment that could affect immune function (including continuous renal replacement therapy,CRRT).
Alcoholic and drug abuse.
Tendency for major mental disease or treatment of anti psychotics.
Pregnant,lactation woman.
Unwilling to assign the informed consent or bad compliance. -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuhang Ai, Doctor.
Organizational Affiliation
Xiangya Hospital of Central South University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Effect of Midazolam on Inflammatory Response and Organ Function in Mechanically Ventilated Sepsis Patients With Different Immune Status
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