Effect of Treatment With Stress-Doses Glucocorticoid in Patients With Acute Respiratory Distress Syndrome (ARDS)
Primary Purpose
Acute Respiratory Distress Syndrome, Adrenal Insufficiency
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
hydrocortisone
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Acute Respiratory Distress Syndrome focused on measuring acute respiratory distress syndrome, glucocorticoid, adrenal insufficiency
Eligibility Criteria
Inclusion Criteria:
- within the first 3 days of onset of clinically definite ARDS confirmed by AECC criteria in 1994
- 18 to 85 year old
Exclusion Criteria:
- pregnancy or lactation
- tumor or other immunologic disease
- immunosuppressive drug used
- bone marrow or lung transplantation
- primary or secondary disease of adrenal gland
- hormone used within 3 months
- refusing conventional therapy
- be in other clinical tests within 30 days
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Placebo Comparator
Active Comparator
Placebo Comparator
Arm Label
glucocorticoid+RAI
placebo + RAI
glucocorticoid
placebo
Arm Description
stress-dose glucocorticoid treatment, compared to placebo group and ACTH test hints RAI
no glucocorticoid But ATCH test hints RAI
stress-dose glucocorticoid treatment, compared to placebo group and ACTH test does not hint RAI
no glucocorticoid But ATCH test does not hint RAI
Outcomes
Primary Outcome Measures
Evidence of clinically definite ARDS confirmed by AECC criteria in 1994
Secondary Outcome Measures
Full Information
NCT ID
NCT00773058
First Posted
October 14, 2008
Last Updated
February 17, 2009
Sponsor
Southeast University, China
Collaborators
Nanjing Medical University
1. Study Identification
Unique Protocol Identification Number
NCT00773058
Brief Title
Effect of Treatment With Stress-Doses Glucocorticoid in Patients With Acute Respiratory Distress Syndrome (ARDS)
Official Title
Effect of Treatment With Stress-Doses Glucocorticoid on Mortality in Patients With ARDS and Relative Adrenal Insufficiency
Study Type
Interventional
2. Study Status
Record Verification Date
January 2009
Overall Recruitment Status
Unknown status
Study Start Date
December 2008 (undefined)
Primary Completion Date
April 2009 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Southeast University, China
Collaborators
Nanjing Medical University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to see if stress doses of hydrocortisone improve early outcome in patients who are in early stage of ARDS and with relative adrenal insufficiency.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome, Adrenal Insufficiency
Keywords
acute respiratory distress syndrome, glucocorticoid, adrenal insufficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
glucocorticoid+RAI
Arm Type
Active Comparator
Arm Description
stress-dose glucocorticoid treatment, compared to placebo group and ACTH test hints RAI
Arm Title
placebo + RAI
Arm Type
Placebo Comparator
Arm Description
no glucocorticoid But ATCH test hints RAI
Arm Title
glucocorticoid
Arm Type
Active Comparator
Arm Description
stress-dose glucocorticoid treatment, compared to placebo group and ACTH test does not hint RAI
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
no glucocorticoid But ATCH test does not hint RAI
Intervention Type
Drug
Intervention Name(s)
hydrocortisone
Other Intervention Name(s)
glucocorticoid, cortical hormone
Intervention Description
hydrocortisone 100mg q8h
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
normal saline 100ml q8h
Primary Outcome Measure Information:
Title
Evidence of clinically definite ARDS confirmed by AECC criteria in 1994
Time Frame
within the first 3 days after surgery onset of ARDS
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
within the first 3 days of onset of clinically definite ARDS confirmed by AECC criteria in 1994
18 to 85 year old
Exclusion Criteria:
pregnancy or lactation
tumor or other immunologic disease
immunosuppressive drug used
bone marrow or lung transplantation
primary or secondary disease of adrenal gland
hormone used within 3 months
refusing conventional therapy
be in other clinical tests within 30 days
12. IPD Sharing Statement
Learn more about this trial
Effect of Treatment With Stress-Doses Glucocorticoid in Patients With Acute Respiratory Distress Syndrome (ARDS)
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