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NCT01861743 · ClinicalTrials.gov registry record · NA

Multimodal Analgesia Versus Routine Care Pain Management

A NA study, sponsored by Rush University Medical Center.

Terminated
Registry status
NA
Development phase
42
Enrollment target

NCT01861743 is a NA study that was terminated before completion, run by Rush University Medical Center. The registered enrollment target is 42 participants.

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The verdict

NCT01861743, a NA study, was terminated before completion, sponsored by Rush University Medical Center.

TERMINATED
Registry status
NA
Development phase
42 participants
Enrollment target

Study Summary

Most patients undergoing surgery experience significant post-operative pain. Inadequate peri-operative pain management may decrease post-operative mobilization and increase length of hospitalization. Additionally, poorly managed acute post-operative pain analgesia is associated with an increased risk of developing chronic pain and delayed wound healing. Lumbar spine surgery is particularly painful, often requiring a multi-day hospitalization. The most common post-operative analgesia used in spine surgery is narcotic medication delivered via an intravenous patient controlled analgesia (IV PCA). A multimodal peri-operative pain management protocol for spine surgery has the potential to not only decrease pain but also to improve recovery, decrease narcotic consumption, decrease length of stay in the hospital and reduce both direct and indirect hospital costs. The purpose of this study is to determine if post-operative pain and rate of recovery are improved in patients undergoing spine surgery using MMA compared to usual analgesic care.

Interventions

  • OTHER Multimodal Analgesia
  • OTHER Patient controlled analgesia

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2013-04
Est. Completion 2017-12
Phase NA

Sponsor

Rush University Medical Center

320 total trials

What the Registry Record Tells You About NCT01861743

The ClinicalTrials.gov registry entry for NCT01861743 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 Rush University Medical Center, which has 320 total studies on file at ClinicalTrials.gov.

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

NCT01861743 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01861743 about?

NCT01861743 is a clinical study titled "Multimodal Analgesia Versus Routine Care Pain Management". Most patients undergoing surgery experience significant post-operative pain. Inadequate peri-operative pain management may decrease post-operative mobilization and increase length of hospitalization. Additionally, poorly managed acute post-operative pain analgesia is associated with an increased ris...

What is the current status of trial NCT01861743?

This trial is currently terminated. It is a NA study. The enrollment target is 42 participants. The study started on 2013-04. Estimated completion is 2017-12.

What interventions are being tested in trial NCT01861743?

The interventions under investigation include: Multimodal Analgesia (OTHER), Patient controlled analgesia (OTHER).

Who is sponsoring clinical trial NCT01861743?

This trial is sponsored by Rush University Medical Center, which has 320 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.