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NCT03133845 · ClinicalTrials.gov registry record · NA

Shaping Anesthetic Techniques to Reduce Post-operative Delirium

A NA study of Delirium and Lumbar Radiculopathy, sponsored by Johns Hopkins University.

Completed
Registry status
NA
Development phase
218
Enrollment target
1
Study location

NCT03133845 is a NA study of Delirium and Lumbar Radiculopathy that has completed, run by Johns Hopkins University. The registered enrollment target is 218 participants, below the 884-participant average among 62 other Delirium trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03133845, a NA study of Delirium and Lumbar Radiculopathy, has completed, sponsored by Johns Hopkins University.

COMPLETED
Registry status
NA
Development phase
218 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine if light sedation with spinal anesthesia reduces the incidence of delirium compared to receiving general anesthesia during spinal surgery in older adults.

Interventions

  • PROCEDURE Light sedation with propofol
  • PROCEDURE Induction with propofol
  • PROCEDURE Maintenance anesthetic using a volatile anesthetic
  • PROCEDURE Muscle relaxant during maintenance anesthesia
  • PROCEDURE Pain control with fentanyl

Study Locations (1)

Maryland

  • Mercy Medical Center - Baltimore

Trial Details

FieldValue
Enrollment Target 218 participants
Start Date 2015-10
Est. Completion 2020-05-25
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT03133845

The ClinicalTrials.gov registry entry for NCT03133845 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 218 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 884-participant average among 62 other Delirium trials with a reported enrollment target (75% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Delirium appearing as the primary indexed condition, and to 5 interventions - of which Light sedation with propofol is the first listed.

NCT03133845 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT03133845 about?

NCT03133845 is a clinical study titled "Shaping Anesthetic Techniques to Reduce Post-operative Delirium". The purpose of this study is to determine if light sedation with spinal anesthesia reduces the incidence of delirium compared to receiving general anesthesia during spinal surgery in older adults.

What is the current status of trial NCT03133845?

This trial is currently completed. It is a NA study. The enrollment target is 218 participants. The study started on 2015-10. Estimated completion is 2020-05-25.

What conditions does trial NCT03133845 study?

This clinical trial studies the following conditions: Delirium, Lumbar Radiculopathy, Lumbar Osteoarthritis, Lumbar Spine Disc Degeneration.

What interventions are being tested in trial NCT03133845?

The interventions under investigation include: Light sedation with propofol (PROCEDURE), Induction with propofol (PROCEDURE), Maintenance anesthetic using a volatile anesthetic (PROCEDURE), Muscle relaxant during maintenance anesthesia (PROCEDURE), Pain control with fentanyl (PROCEDURE).

Who is sponsoring clinical trial NCT03133845?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03133845 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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