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Trial · NCT00862381

Hydrocortisone Use After Etomidate in Intensive Care

NCT00862381, Phase 3, Completed, University Hospital, Grenoble

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Hydrocortisone Use After Etomidate in Intensive Care. Trials, record NCT00862381. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00862381

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Hydrocortisone Use After Etomidate in Intensive Care
NCT number
NCT00862381
Status
Completed
Phases
Phase 3
Enrollment
106 participants, actual
Lead sponsor
University Hospital, Grenoble
Conditions
Patient Admitted in Reanimation
Interventions
Hydrocortisone, Placebo
First posted
2009-03-16
Last updated
2010-07-26

Source ClinicalTrials.gov

Registered outcomes10

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primarydiminution of 50% of the proportion of patients with a score SOFA of 3 or 412h, 24h and 48h after the injection of hydrocortisone
Primarymean arterial blood pressureduring the hospitalisation
Primaryplasmatic cortisol and substance S before and after ACTH stimulationh-4; h6; h12 and h24
Secondaryclinical state12h and 24h
Secondaryhospitalisation duration in reanimationuntil day28
Secondaryduration of mechanical ventilationuntil day28
Secondaryduration and posology of adrenaline and noradrenalineh0, h4, h6, h12, h24 and h48
Secondarycomplications during hospitalization in reanimation potentially due to HSHCuntil day28
Secondarydose of etomidate injectionh0
Secondarymortalityday28

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
21926601DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00862381

GET https://conductscience.org/api/trials/v1/NCT00862381/registered