Mechanistic Assessment of Norepinephrine Therapy vs. Angiotensin-II in Septic Shock

ConditionSeptic Shock
Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorWake Forest University Health Sciences

About this trial

Despite best therapy efforts, sepsis and septic shock are associated with mortality rates of up to 40%. This clinical trial will determine the benefit of exogenous Angiotensin II versus norepinephrine (conventional care) treatment in septic shock patients. This trial will determine whether there are better predictors of septic shock severity. This approach may inform more appropriate treatment regimens and improve outcomes for these patients.

Eligibility criteria

Qualifiers

None

Disqualifiers

Age <18 years

Prisoners

Pregnant women

Patients for whom urgent surgery is anticipated

Trial design

Treatments tested in this trial

  • Angiotensin II
  • Norepinephrine

Treatment groups

78 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Wake Forest University Health Sciences

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator