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NCT05221866 · ClinicalTrials.gov registry record · NA

Efficiency And Quality In Post-Surgical Pain Therapy After Discharge

A NA study, sponsored by University of Nebraska.

Completed
Registry status
NA
Development phase
711
Enrollment target

NCT05221866 is a NA study that has completed, run by University of Nebraska. The registered enrollment target is 711 participants.

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The verdict

NCT05221866, a NA study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
NA
Development phase
711 participants
Enrollment target

Study Summary

Following inpatient surgery, more than 80% of patients are prescribed opioids for use after discharge, yet up to 90% of patients report leftover opioids, and only 16% maximize non-opioid therapy. The proposed study seeks to test a provider-facing decision support tool and a participant-facing smartphone app to reduce the amount of opioids prescribed and taken following discharge, while ensuring effective treatment of pain after surgery. Adult participants with smart phones having had inpatient surgery requiring at least over-night hospitalization with anticipated discharge to home will be randomized to one of the two groups. Study measurements will include self-reported cumulative amounts of opioids taken after discharge, non-opioid analgesic taken, prescribed post-discharge opioid doses in morphine milligram equivalents (MME), pain intensity and pain interference scores (PROMIS), need for additional opioid prescriptions within one-month post-discharge, as well as any self-reported disposal of leftover medications.

Interventions

  • BEHAVIORAL Empowering Patient to Steer Their Pain Management After Surgery
  • BEHAVIORAL Provider-facing Prescription Aid

Trial Details

FieldValue
Enrollment Target 711 participants
Start Date 2022-05-02
Est. Completion 2023-12-10
Phase NA

Sponsor

University of Nebraska

407 total trials

What the Registry Record Tells You About NCT05221866

The ClinicalTrials.gov registry entry for NCT05221866 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 711 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Nebraska, which has 407 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Empowering Patient to Steer Their Pain Management After Surgery is the first listed.

NCT05221866 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05221866 about?

NCT05221866 is a clinical study titled "Efficiency And Quality In Post-Surgical Pain Therapy After Discharge". Following inpatient surgery, more than 80% of patients are prescribed opioids for use after discharge, yet up to 90% of patients report leftover opioids, and only 16% maximize non-opioid therapy. The proposed study seeks to test a provider-facing decision support tool and a participant-facing smartp...

What is the current status of trial NCT05221866?

This trial is currently completed. It is a NA study. The enrollment target is 711 participants. The study started on 2022-05-02. Estimated completion is 2023-12-10.

What interventions are being tested in trial NCT05221866?

The interventions under investigation include: Empowering Patient to Steer Their Pain Management After Surgery (BEHAVIORAL), Provider-facing Prescription Aid (BEHAVIORAL).

Who is sponsoring clinical trial NCT05221866?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

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

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