Clinical Trials Directory

Trials / Terminated

TerminatedNCT01722422

Hyperoxia and Hypertonic Saline in Septic Shock

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
441 (actual)
Sponsor
University Hospital, Angers · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Assessment of the effect of hyperoxia and hypertonic saline on survival in patients with septic shock Hyperoxia and hypertonic saline may have beneficial effects on organ perfusion and oxygenation and may reduce the organ failure occurences. To date, only scarce data are available. Side effects are not well described. Therefore we designed a randomized clinical trial in order to assess the early administration of hypertonic saline and oxygen in the very early beginning of septic shock.

Detailed description

The study is designed as factorial 2x2. Patients will be stratified at the randomisation according the presence or absence of Acute Respiratory Distress Syndrome in order to perform a sub group analysis for all outcome criteria.

Conditions

Interventions

TypeNameDescription
DRUGoxygen and saline

Timeline

Start date
2012-10-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2012-11-06
Last updated
2014-11-20

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01722422. Inclusion in this directory is not an endorsement.