Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00455143 · ClinicalTrials.gov registry record · Phase 4

Cognitive Protection - Dexmedetomidine and Cognitive Reserve

A Phase 4 study, sponsored by Icahn School of Medicine at Mount Sinai.

Terminated
Registry status
Phase 4
Development phase
27
Enrollment target

NCT00455143: Clinical Trial Phase 4 study, sponsored by Icahn School of Medicine at Mount Sinai.

NCT00455143 is a Phase 4 study that was terminated before completion, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 27 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00455143, a Phase 4 study, was terminated before completion, sponsored by Icahn School of Medicine at Mount Sinai.

TERMINATED
Registry status
Phase 4
Development phase
27 participants
Enrollment target

Study Summary

This is a pilot study to evaluate the effect of dexmedetomidine in the prevention of delirium in non-cardiac surgical patients. The preliminary data regarding the effect of dexmedetomidine on delirium comes from a study underway at Stanford. We propose to randomize fifty patients into two different protocols, one using dexmedetomidine until PACU discharge (hip replacement) and the other using dexmedetomidine for 24 hours in a monitored setting.

Interventions

  • DRUG Placebo
  • DRUG Precedex (Dexmedetomidine)

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2006-09
Est. Completion 2009-04
Phase Phase 4

Why NCT00455143 stopped before completion

NCT00455143 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00455143 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00455143 about?

NCT00455143 is a clinical study titled "Cognitive Protection - Dexmedetomidine and Cognitive Reserve". This is a pilot study to evaluate the effect of dexmedetomidine in the prevention of delirium in non-cardiac surgical patients. The preliminary data regarding the effect of dexmedetomidine on delirium comes from a study underway at Stanford. We propose to randomize fifty patients into two different ...

What is the current status of trial NCT00455143?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 27 participants. The study started on 2006-09. Estimated completion is 2009-04.

What interventions are being tested in trial NCT00455143?

The interventions under investigation include: Placebo (DRUG), Precedex (Dexmedetomidine) (DRUG).

Who is sponsoring clinical trial NCT00455143?

This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00455143's enrollment target sits among peer trials

27 1651st of 2000 higher than 346 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00912041 · 27 participants · NA

    BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia

  • NCT02847559 · 27 participants · Phase 2

    Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma

  • NCT03380195 · 27 participants · NA

    Effects of Watermelon Juice on Heart Rate Recovery and Post-exercise Muscle Soreness

  • NCT03384238 · 27 participants · Phase 1

    Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00455143, the US trial registry maintained by the National Library of Medicine. NCT00455143 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.