Stress Doses of Hydrocortisone on Coagulation Dysfunction in Patients With Septic Shock
Information source: Nanjing PLA General Hospital
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Septic Shock; Sepsis
Intervention: Hydrocortisone (Drug)
Phase: Phase 3
Status: Completed
Sponsored by: Nanjing PLA General Hospital
Summary
The purpose of this study is to find out whether stress doses of hydrocortisone attenuate
coagulation dysfunction in patients with septic shock. And discuss the probable mechanism by
which little doses of hydrocortisone influence coagulation system in sepsis.
Clinical Details
Official title: Research of Little Doses of Hydrocortisone on Coagulation Dysfunction in Patients With Septic Shock
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: coagulopathy
Secondary outcome: deathclinical complications
Detailed description:
Patients were randomized to receive either low-dose hydrocortisone or matching
placebo. Severity of coagulopathy was estimated using ISTH DIC score. We determined the
complications and mortality in two groups, and analyzed the relationship between
hydrocortisone and coagulopathy.
Eligibility
Minimum age: 18 Years.
Maximum age: 80 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- All patients(ageā§18y)
- Admitted for septic shock were considered eligible if they had no life-threatening
systemic disease (ASA groups 1~3)
Exclusion Criteria:
- Lactation
- Mental disorders
- Disseminated cancer
- Secondary cancers
- Inflammatory bowel disease, or diseases hindering epidural analgesia
Locations and Contacts
Additional Information
Starting date: November 2011
Last updated: October 16, 2014
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