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NCT04015908 · ClinicalTrials.gov registry record · Phase 4

A Multimodal Analgesia Protocol Adapted for Ambulatory Surgery

A Phase 4 study, sponsored by University of Utah.

Completed
Registry status
Phase 4
Development phase
100
Enrollment target

NCT04015908 is a Phase 4 study that has completed, run by University of Utah. The registered enrollment target is 100 participants.

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The verdict

NCT04015908, a Phase 4 study, has completed, sponsored by University of Utah.

COMPLETED
Registry status
Phase 4
Development phase
100 participants
Enrollment target

Study Summary

The primary objective of this trial is to determine whether the combination of three non-opioid analgesics (multimodal analgesia) can significantly reduce or eliminate the need for opioids after ambulatory surgery. A secondary objective would be to present credible data for insurance providers about the opioid sparing effect of these medications. This data may encourage insurance providers to support payment for short term use of certain analgesics that currently require prior authorization.

Interventions

  • DRUG Acetaminophen
  • DRUG Celecoxib
  • DRUG Oxycodone
  • DRUG Pregabalin
  • DRUG Percocet

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2019-08-01
Est. Completion 2023-01-31
Phase Phase 4

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT04015908

The ClinicalTrials.gov registry entry for NCT04015908 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Acetaminophen is the first listed.

NCT04015908 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04015908 about?

NCT04015908 is a clinical study titled "A Multimodal Analgesia Protocol Adapted for Ambulatory Surgery". The primary objective of this trial is to determine whether the combination of three non-opioid analgesics (multimodal analgesia) can significantly reduce or eliminate the need for opioids after ambulatory surgery. A secondary objective would be to present credible data for insurance providers abou...

What is the current status of trial NCT04015908?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2019-08-01. Estimated completion is 2023-01-31.

What interventions are being tested in trial NCT04015908?

The interventions under investigation include: Acetaminophen (DRUG), Celecoxib (DRUG), Oxycodone (DRUG), Pregabalin (DRUG), Percocet (DRUG).

Who is sponsoring clinical trial NCT04015908?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

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

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.