Clinical Trials Directory

Trials / Terminated

TerminatedNCT01856517

Upregulation of Alpha-1 Receptors Upon Septic Shock?

Up Regulation of Alpha-1 Receptors Upon Septic Shock ?

Status
Terminated
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Direction Centrale du Service de Santé des Armées · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The hallmarks of septic shock are hypovolemia and reduced pressor response to endogenous noradrenaline. The working hypothesis is that the higher the plasma concentration of endogenous noradrenaline will be, the lower the pressor response to exogenous noradrenaline will be. This will be tested in patients presenting with septic shock, following state of the art management (including repeated assessment of vena cava diameter and compliance, and response to dynamic indices of loading) following placebo vs clonidine administration (1 mcg.kg-1.h-1 over 24 h without bolus) and administration of increasing doses of noradrenaline (1 mcg, 2 mcg, etc. up to a delta systolic blood pressure circa 25-30 mm Hg).

Conditions

Interventions

TypeNameDescription
DRUGClonidine
DRUGPlacebo

Timeline

Start date
2013-08-01
Primary completion
2013-08-01
Completion
2014-09-01
First posted
2013-05-17
Last updated
2017-07-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01856517. Inclusion in this directory is not an endorsement.