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NCT04043143 · ClinicalTrials.gov registry record · NA

24-hour Oral Morphine Equivalent Based Opioid Prescribing After Surgery

A NA study, sponsored by University of Colorado, Denver.

Completed
Registry status
NA
Development phase
57
Enrollment target

NCT04043143 is a NA study that has completed, run by University of Colorado, Denver. The registered enrollment target is 57 participants.

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The verdict

NCT04043143, a NA study, has completed, sponsored by University of Colorado, Denver.

COMPLETED
Registry status
NA
Development phase
57 participants
Enrollment target

Study Summary

The investigators will utilize the electronic health record to individualize pain therapy in surgical patients after hospital discharge using last 24-hour opioid intake as the decision variable for the amount of opioid pain pills prescribed. The preliminary data indicate that current opioid prescription practice after surgery follows a "one size fits all" pattern. In-hospital opioid use 24 hours prior to discharge serves as a strong indicator to correctly estimate needs for analgesic medications at home. The investigators will test the hypothesis that this prescription estimation tool will enable providers to write need-based prescriptions based on each patient's' 24-hour prior-to-discharge opioid use. The investigators will test this tool prospectively for patients after Cesarean section who are anticipated to use about half or less of the usually prescribed amount of opioid pain pills after discharge randomized equally to prescription tool intervention or no intervention (prescription as usual).

Interventions

  • OTHER Arm 1 Prescription As Usual
  • OTHER Arm 2 Prescription Tool Intervention

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2019-10-24
Est. Completion 2021-01-13
Phase NA

Sponsor

University of Colorado, Denver

1,283 total trials

What the Registry Record Tells You About NCT04043143

The ClinicalTrials.gov registry entry for NCT04043143 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Arm 1 Prescription As Usual is the first listed.

NCT04043143 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04043143 about?

NCT04043143 is a clinical study titled "24-hour Oral Morphine Equivalent Based Opioid Prescribing After Surgery". The investigators will utilize the electronic health record to individualize pain therapy in surgical patients after hospital discharge using last 24-hour opioid intake as the decision variable for the amount of opioid pain pills prescribed. The preliminary data indicate that current opioid prescrip...

What is the current status of trial NCT04043143?

This trial is currently completed. It is a NA study. The enrollment target is 57 participants. The study started on 2019-10-24. Estimated completion is 2021-01-13.

What interventions are being tested in trial NCT04043143?

The interventions under investigation include: Arm 1 Prescription As Usual (OTHER), Arm 2 Prescription Tool Intervention (OTHER).

Who is sponsoring clinical trial NCT04043143?

This trial is sponsored by University of Colorado, Denver, which has 1,283 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.