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NCT05658796 · ClinicalTrials.gov registry record · NA

RXWell to Decrease Post-Operative Opioid Use in Total Knee or Hip Arthroplasty

A NA study of Depression and Anxiety, sponsored by University of Pittsburgh.

Recruiting
Registry status
NA
Development phase
150
Enrollment target
3
Study locations

NCT05658796: Recruiting NA study of Depression and Anxiety, sponsored by University of Pittsburgh.

NCT05658796 is a NA study of Depression and Anxiety that is actively recruiting participants, run by University of Pittsburgh. The registered enrollment target is 150 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (81% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05658796, a NA study of Depression and Anxiety, is actively recruiting participants, sponsored by University of Pittsburgh.

RECRUITING
Registry status
NA
Development phase
150 participants
Enrollment target
3
Study locations

Study Summary

It is envisioned that multipronged benefits from this pilot work for the UPMC ISD and its members. It is expected the RxWell platform to provide the following benefits: expansion of the use of RxWell to all UPMC ISD members providing peri-operative mood management with advantage of improved peri-operative outcomes, improving saving for the UPMC ISD by hastening the recovery and decreased resource utilization, and addition to the high-value care of UPMC with this holistic approach to patient perioperative care

Primary Outcome

This outcome will be measured by extracting pain medication data from the electronic health record to determine OME (oral morphine equivalents) (mg) for opioid medications on POD 1 and 2, and weeks 1 and 4 following surgery. This will be recorded for each study arm as mean (SD).

Interventions

  • BEHAVIORAL +RxWell
  • BEHAVIORAL -RxWell

Study Locations (3)

Pennsylvania

  • UPMC East - Monroeville
  • UPMC Shadyside - Pittsburgh
  • UPMC Passavant - Pittsburgh

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2023-01-27
Est. Completion 2026-12-30
Phase NA
University of Pittsburgh

1,238 total trials

What NCT05658796 shows while recruiting

NCT05658796 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 786-participant average among 679 other Depression trials with a reported enrollment target (81% lower).

The record links to 6 conditions, with Depression appearing as the primary indexed condition, and to 2 interventions - of which +RxWell is the first listed.

NCT05658796 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05658796 about?

NCT05658796 is a clinical study titled "RXWell to Decrease Post-Operative Opioid Use in Total Knee or Hip Arthroplasty". It is envisioned that multipronged benefits from this pilot work for the UPMC ISD and its members. It is expected the RxWell platform to provide the following benefits: expansion of the use of RxWell to all UPMC ISD members providing peri-operative mood management with advantage of improved peri-ope...

What is the current status of trial NCT05658796?

This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2023-01-27. Estimated completion is 2026-12-30.

What conditions does trial NCT05658796 study?

This clinical trial studies the following conditions: Depression, Anxiety, Anxiety Disorders, Depressive Symptoms, Mood Disorders.

What interventions are being tested in trial NCT05658796?

The interventions under investigation include: +RxWell (BEHAVIORAL), -RxWell (BEHAVIORAL).

Who is sponsoring clinical trial NCT05658796?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05658796 being conducted?

This trial has 3 study locations across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Depression

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05658796's enrollment target sits among peer trials

150 249th of 679 higher than 416 of 679 other Depression trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Depression trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05658796, the US trial registry maintained by the National Library of Medicine. NCT05658796 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.