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NCT00952081 · ClinicalTrials.gov registry record · Phase 4

A Pilot Study to Evaluate Efficacy and Safety of Clevidipine in Neurosurgical Patients

A Phase 4 study, sponsored by NYU Langone Health.

Completed
Registry status
Phase 4
Development phase
22
Enrollment target

NCT00952081: Completed Phase 4 study, sponsored by NYU Langone Health.

NCT00952081 is a Phase 4 study that has completed, run by NYU Langone Health. The registered enrollment target is 22 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00952081, a Phase 4 study, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
Phase 4
Development phase
22 participants
Enrollment target

Study Summary

This protocol describes a study to gain experience in the use of Clevidipine for perioperative blood pressure control in patients undergoing craniotomy for brain tumor or epilepsy focus resection. The purpose of this study is to establish the efficacy of Clevidipine for intraoperative blood pressure control in patients undergoing intracranial procedures, and gather information on the dosage and adverse effects of Clevidipine in neurosurgical patients. This initial pilot experience serves to familiarize the investigators with the use of this drug prior to initiating a planned randomized trial versus institutional standard-of-care therapy. The investigators will obtain greater familiarity with the dosing of clevidipine in this patient population and collect information on the incidence of adverse effects.

Interventions

  • DRUG Clevidipine

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2009-07
Est. Completion 2010-02
Phase Phase 4
NYU Langone Health

1,164 total trials

What the finished NCT00952081 record still lists

NCT00952081 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

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

NCT00952081 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00952081 about?

NCT00952081 is a clinical study titled "A Pilot Study to Evaluate Efficacy and Safety of Clevidipine in Neurosurgical Patients". This protocol describes a study to gain experience in the use of Clevidipine for perioperative blood pressure control in patients undergoing craniotomy for brain tumor or epilepsy focus resection. The purpose of this study is to establish the efficacy of Clevidipine for intraoperative blood pressure...

What is the current status of trial NCT00952081?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 22 participants. The study started on 2009-07. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00952081?

The interventions under investigation include: Clevidipine (DRUG).

Who is sponsoring clinical trial NCT00952081?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00952081's enrollment target sits among peer trials

22 1731st of 2000 higher than 259 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

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Source: ClinicalTrials.gov NCT00952081, the US trial registry maintained by the National Library of Medicine. NCT00952081 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.