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NCT03325972 · ClinicalTrials.gov registry record · Phase 4

Study on the Effects of Intravenous Dexmedetomidine on Pain in Patients Undergoing Elective Spinal Surgery

A Phase 4 study, sponsored by NYU Langone Health.

Completed
Registry status
Phase 4
Development phase
83
Enrollment target

NCT03325972 is a Phase 4 study that has completed, run by NYU Langone Health. The registered enrollment target is 83 participants.

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The verdict

NCT03325972, a Phase 4 study, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
Phase 4
Development phase
83 participants
Enrollment target

Study Summary

This is a randomized, prospective, double-blind , placebo-controlled trial examining the effects of intraoperative dexmedetomidine infusion on pain in patients undergoing lumbar spinal fusion surgery. One hundred ten subjects (55 in each arm) will be enrolled. Subjects, over the age of 18, undergoing lumbar spinal fusion will be considered eligible for enrollment. Subjects will receive either intraoperative dexmedetomidine or placebo of normal saline infusion. They will be followed for approximately six weeks postoperatively.

Interventions

  • DRUG Dexmedetomidine
  • OTHER Placebo Saline

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2016-09-14
Est. Completion 2022-02-22
Phase Phase 4

Sponsor

NYU Langone Health

1,164 total trials

What the Registry Record Tells You About NCT03325972

The ClinicalTrials.gov registry entry for NCT03325972 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 83 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.

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

NCT03325972 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03325972 about?

NCT03325972 is a clinical study titled "Study on the Effects of Intravenous Dexmedetomidine on Pain in Patients Undergoing Elective Spinal Surgery". This is a randomized, prospective, double-blind , placebo-controlled trial examining the effects of intraoperative dexmedetomidine infusion on pain in patients undergoing lumbar spinal fusion surgery. One hundred ten subjects (55 in each arm) will be enrolled. Subjects, over the age of 18, undergoin...

What is the current status of trial NCT03325972?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 83 participants. The study started on 2016-09-14. Estimated completion is 2022-02-22.

What interventions are being tested in trial NCT03325972?

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

Who is sponsoring clinical trial NCT03325972?

This trial is sponsored by NYU Langone Health, which has 1,164 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.