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NCT00842933 · ClinicalTrials.gov registry record · Phase 4

Adrenal Insufficiency in Septic Shock

A Phase 4 study, sponsored by The Methodist Hospital Research Institute.

Terminated
Registry status
Phase 4
Development phase
32
Enrollment target

NCT00842933 is a Phase 4 study that was terminated before completion, run by The Methodist Hospital Research Institute. The registered enrollment target is 32 participants.

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The verdict

NCT00842933, a Phase 4 study, was terminated before completion, sponsored by The Methodist Hospital Research Institute.

TERMINATED
Registry status
Phase 4
Development phase
32 participants
Enrollment target

Study Summary

Randomized controlled trial evaluating the duration of steroid replacement therapy in patients with adrenal insufficiency and septic shock. Patients will be randomized to receive either hydrocortisone 50 mg IV every six hours for seven days (control) or hydrocortisone 50 mg IV every six hours until 24 hours after achievement of hemodynamic stability (MAP \> 65 mm Hg off of vasopressors).

Interventions

  • DRUG Corticosteroid

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2007-05
Est. Completion 2011-05
Phase Phase 4

What the Registry Record Tells You About NCT00842933

The ClinicalTrials.gov registry entry for NCT00842933 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Corticosteroid is the first listed.

NCT00842933 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00842933 about?

NCT00842933 is a clinical study titled "Adrenal Insufficiency in Septic Shock". Randomized controlled trial evaluating the duration of steroid replacement therapy in patients with adrenal insufficiency and septic shock. Patients will be randomized to receive either hydrocortisone 50 mg IV every six hours for seven days (control) or hydrocortisone 50 mg IV every six hours until ...

What is the current status of trial NCT00842933?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 32 participants. The study started on 2007-05. Estimated completion is 2011-05.

What interventions are being tested in trial NCT00842933?

The interventions under investigation include: Corticosteroid (DRUG).

Who is sponsoring clinical trial NCT00842933?

This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.