HCT+F vs. HCT Alone in Critically Ill Medical Septic Shock Patients

Completed · Phase 2

Conditions studied: Septic Shock

In brief

This study will be conducted as a single-center, prospective, open-label, randomized trial that will evaluate adult patients admitted with septic shock to the medical critical care unit (MCC). The objective of the study is to determine if the use of hydrocortisone plus fludrocortisone is associated with a faster resolution of shock (defined as 24 hours vasopressor free) when compared to the use of hydrocortisone alone in medical, critically ill septic shock patients.

Key facts

Study ID
NCT03710187
Run by
University of Tennessee Medical Center
People needed
84
Starts
2018-11-05
Expected to finish
2019-09-27
Last updated by the study team
2021-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.