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NCT03858231 · ClinicalTrials.gov registry record · Phase 4

Opioids Versus Non-Opioids Postoperative After Knee Arthroscopic Surgery

A Phase 4 study of Pain, Postoperative and Opioid Use, sponsored by Sanford Health.

Recruiting
Registry status
Phase 4
Development phase
148
Enrollment target
1
Study location

NCT03858231 is a Phase 4 study of Pain, Postoperative and Opioid Use that is actively recruiting participants, run by Sanford Health. The registered enrollment target is 148 participants, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (45% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03858231, a Phase 4 study of Pain, Postoperative and Opioid Use, is actively recruiting participants, sponsored by Sanford Health.

RECRUITING
Registry status
Phase 4
Development phase
148 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to look at pain management with opioids versus non-opioids after knee arthroscopy. This study will determine 1) whether the most commonly used non-narcotic medications provide pain relief comparable with the most commonly prescribed narcotic medications in patients undergoing arthroscopic knee surgery, and 2) whether patients' characteristics (gender, pre-operative knee symptoms, workers compensation status and employment status) affect pain level following surgery or medication usage.

Conditions Studied

Pain, Postoperative Opioid Use Knee Injuries

Interventions

  • DRUG Ibuprofen 600 mg
  • DRUG Norco 5Mg-325Mg Tablet
  • DRUG Acetaminophen 325Mg Tab

Study Locations (1)

North Dakota

  • Sanford Health - Fargo

Trial Details

FieldValue
Enrollment Target 148 participants
Start Date 2018-10-29
Est. Completion 2028-01
Phase Phase 4

Sponsor

Sanford Health

34 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03858231

The ClinicalTrials.gov registry entry for NCT03858231 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 148 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (45% lower). The listed sponsor is Sanford Health, which has 34 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 3 interventions - of which Ibuprofen 600 mg is the first listed.

NCT03858231 reports 1 study location spanning 1 distinct geographic area - top geographies include North Dakota.

Frequently Asked Questions

What is clinical trial NCT03858231 about?

NCT03858231 is a clinical study titled "Opioids Versus Non-Opioids Postoperative After Knee Arthroscopic Surgery". The purpose of this study is to look at pain management with opioids versus non-opioids after knee arthroscopy. This study will determine 1) whether the most commonly used non-narcotic medications provide pain relief comparable with the most commonly prescribed narcotic medications in patients under...

What is the current status of trial NCT03858231?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 148 participants. The study started on 2018-10-29. Estimated completion is 2028-01.

What conditions does trial NCT03858231 study?

This clinical trial studies the following conditions: Pain, Postoperative, Opioid Use, Knee Injuries.

What interventions are being tested in trial NCT03858231?

The interventions under investigation include: Ibuprofen 600 mg (DRUG), Norco 5Mg-325Mg Tablet (DRUG), Acetaminophen 325Mg Tab (DRUG).

Who is sponsoring clinical trial NCT03858231?

This trial is sponsored by Sanford Health, which has 34 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03858231 being conducted?

This trial has 1 study location across North Dakota. 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

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.