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NCT03236155 · ClinicalTrials.gov registry record · Phase 4

Comparing Opioid Prescription Patterns in Total Joint Arthroplasty Patients

A Phase 4 study of Postoperative Pain, sponsored by Rush University Medical Center.

Completed
Registry status
Phase 4
Development phase
304
Enrollment target
1
Study location

NCT03236155: Completed Phase 4 study of Postoperative Pain, sponsored by Rush University Medical Center.

NCT03236155 is a Phase 4 study of Postoperative Pain that has completed, run by Rush University Medical Center. The registered enrollment target is 304 participants, above the 229-participant average among 120 other Postoperative Pain trials with a reported enrollment target (33% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03236155, a Phase 4 study of Postoperative Pain, has completed, sponsored by Rush University Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
304 participants
Enrollment target
1
Study location

Study Summary

The United States constitutes \<5% of the world's population but over 80% of the opioid supply and 99% of the hydrocodone supply. In 2014, there were 18,893 deaths from prescription drug overdose, and orthopaedic surgeons are the third highest prescribing physicians for opioids. Surgeons often prescribe opioids to minimize postoperative pain and to reduce the likelihood of readmission for pain. Available data suggests that orthopaedic surgeons are the most likely physicians to prescribe opioids to Medicare patients, whose opioid prescriptions are over 7 times more likely to come from an orthopaedic surgeon than another type of physician, but orthopaedic surgeons also had the highest readmission rate for post-operative pain. Many studies have investigated the utilization of opioids after surgery to assess surgeon's tendencies to overprescribe, demographics of those likely to overuse, and adverse events of opioid abusers. The primary purpose of this randomized controlled trial is to determine whether prescribing fewer opioid pills per prescription reduces the total amount of opioids taken, even while allowing equal total opioid availability via increased frequency of prescription availability.

Primary Outcome

Self-reported by patient, we are asking for the number of Oxycodone taken by patients (5mg doses). This will be verified with patient bringing their pill bottle in and counted by a study investigator.

Conditions Studied

Interventions

  • DRUG opioid pain pills

Study Locations (1)

Illinois

  • Rush University Medical Center - Chicago

Trial Details

FieldValue
Enrollment Target 304 participants
Start Date 2017-07-01
Est. Completion 2018-08-26
Phase Phase 4
Rush University Medical Center

320 total trials

What the finished NCT03236155 record still lists

NCT03236155 is an interventional study that assigns participants to a tested intervention. The registered 304 participants enrollment target is mid-sized for trials with a published cap, above the 229-participant average among 120 other Postoperative Pain trials with a reported enrollment target (33% higher).

The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which opioid pain pills is the first listed.

NCT03236155 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT03236155 about?

NCT03236155 is a clinical study titled "Comparing Opioid Prescription Patterns in Total Joint Arthroplasty Patients". The United States constitutes \<5% of the world's population but over 80% of the opioid supply and 99% of the hydrocodone supply. In 2014, there were 18,893 deaths from prescription drug overdose, and orthopaedic surgeons are the third highest prescribing physicians for opioids. Surgeons often presc...

What is the current status of trial NCT03236155?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 304 participants. The study started on 2017-07-01. Estimated completion is 2018-08-26.

What conditions does trial NCT03236155 study?

This clinical trial studies the following conditions: Postoperative Pain.

What interventions are being tested in trial NCT03236155?

The interventions under investigation include: opioid pain pills (DRUG).

Who is sponsoring clinical trial NCT03236155?

This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03236155 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Postoperative Pain

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 NCT03236155's enrollment target sits among peer trials

304 19th of 120 higher than 102 of 120 other Postoperative Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Postoperative Pain 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 NCT03236155, the US trial registry maintained by the National Library of Medicine. NCT03236155 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.