Clinical Trials Directory

Trials / Completed

CompletedNCT02266589

Stress Doses of Hydrocortisone on Coagulation Dysfunction in Patients With Septic Shock

Research of Little Doses of Hydrocortisone on Coagulation Dysfunction in Patients With Septic Shock

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Nanjing PLA General Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

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.

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.

Conditions

Interventions

TypeNameDescription
DRUGHydrocortisoneHydrocortisone hemisuccinate (Roussel-Uclaf, Romainville, France), 50 mg intravenously every 6 hrs

Timeline

Start date
2011-11-01
Primary completion
2013-10-01
Completion
2013-10-01
First posted
2014-10-17
Last updated
2014-10-17

Source: ClinicalTrials.gov record NCT02266589. Inclusion in this directory is not an endorsement.