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NCT00464490 · ClinicalTrials.gov registry record · NA

Use of Dexmedetomidine to Facilitate Extubation in Surgical ICU Patients Who Failed Previous Weaning Attempts

A NA study, sponsored by University of California, San Francisco.

Terminated
Registry status
NA
Development phase
42
Enrollment target

NCT00464490 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 42 participants.

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The verdict

NCT00464490, a NA study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
NA
Development phase
42 participants
Enrollment target

Study Summary

Mechanical ventilation commonly is associated with patient agitation requiring sedation to alleviate discomfort and reduce excessive central respiratory drive. Upon recovery from acute respiratory failure, sedation is reduced to facilitate the withdrawal of ventilatory support. In some patients, abrupt reduction in sedation provokes severe agitation that causes catecholamine release resulting in severe hypertension, tachycardia and tachypnea. This requires increased sedation to bring hemodynamic and respiratory function under control. Dexmedetomidine is an alpha-2 receptor agonist with both sedative and analgesic properties that allows for the reduction in the anesthetic and analgesic requirements in the perioperative setting. In addition to its sedative effects, alpha-2 receptor stimulation in the central nervous system inhibits sympathetic activity and reduces plasma epinephrine and norepinephrine levels, thereby lowering both arterial blood pressure and heart rate. Because alpha-2 receptor stimulation does not cause respiratory depression, dexmedetomidine may facilitate the transition to unassisted breathing in profoundly agitated patients. The investigators will prospectively evaluate dexmedetomidine in 30 patients who could not be extubated because of agitation with hemodynamic instability and tachypnea. The purpose of this study is to test if a larger prospective randomized controlled pilot study can show that dexmedetomidine facilitates weaning and extubation in patients who have failed previous attempts because of agitation and hyperdynamic cardiopulmonary response.

Interventions

  • DRUG Dexmedetomidine

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2007-11
Est. Completion 2012-12
Phase NA

What the Registry Record Tells You About NCT00464490

The ClinicalTrials.gov registry entry for NCT00464490 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

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

NCT00464490 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00464490 about?

NCT00464490 is a clinical study titled "Use of Dexmedetomidine to Facilitate Extubation in Surgical ICU Patients Who Failed Previous Weaning Attempts". Mechanical ventilation commonly is associated with patient agitation requiring sedation to alleviate discomfort and reduce excessive central respiratory drive. Upon recovery from acute respiratory failure, sedation is reduced to facilitate the withdrawal of ventilatory support. In some patients, abr...

What is the current status of trial NCT00464490?

This trial is currently terminated. It is a NA study. The enrollment target is 42 participants. The study started on 2007-11. Estimated completion is 2012-12.

What interventions are being tested in trial NCT00464490?

The interventions under investigation include: Dexmedetomidine (DRUG).

Who is sponsoring clinical trial NCT00464490?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

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

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.