Back to search results

Nonopioid Pain Control After Fracture Surgery

This study is testing a nonopioid pain control regimen for patients undergoing surgery for traumatic fractures (broken bones). After your surgery, you would either receive standard opioid pain medications or a nonopioid pain control regimen. The goal is to see if the nonopioid regimen can manage pain as effectively as opioids, while minimizing side effects. Researchers will measure your pain scores daily for the first two weeks, then weekly until six weeks after surgery. This study is for adults aged 18 to 80 who are having surgery for a traumatic fracture at Henry Ford Hospital or Henry Ford West Bloomfield Hospital. The current status of this study is unclear.

Study design
This is a randomized, single-blinded study comparing two pain management approaches, with a planned enrollment of 75 participants.
What's involved
You would have your pain scores recorded daily for the first two weeks after surgery, and then once a week until your six-week post-operative clinic visit.
Compensation
Not stated in the trial record.
Follow-up
Pain scores will be measured daily for the first 2 weeks, and then once a week until the 6-week post-operative clinic visit.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06113211

Nonopioid Pain Control Regimen After Open Reduction and Internal Fixation of Traumatic Fractures

Recruiting
PHASE4Ages 18–80InterventionalTreatment
Henry Ford Health System
~75 participants
Updated 2026-04-13 on ClinicalTrials.gov
What's tested:Narcotic pain medicationNonnarcotic pain medications

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Pain Score
Measured over Pain scores will be recorded daily for the first 2 weeks, and then once a week until the 6 week post operative clinic visit.

Conditions

Opioid Use
Fractures, Bone
Trauma

Explore related trials

Fracture

Where it's being run

1 sites across 1 states
Michigan1

Who to contact

William Hakeos
[email protected]
3132055349
Email the study team

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

All adult patients over age eighteen and scheduled for primary open reduction internal fixation following a traumatic fracture at Henry Ford Hospital (Detroit, Michigan, United States), and Henry Ford West Bloomfield Hospital (West Bloomfield, Michigan, United States) will be eligible for inclusion in this study. All patients will be met in our abulatory orthopedic clinics. All surgeries will be performed by a fellowship trained truama surgeons.

Exclusion

patients with a medical history of known allergies or intolerance to allergies or intolerance to Motrin, Lyrica, Tylenol, tramadol, Zanaflex
substantial alcohol or drug abuse
pregnancy
history of narcotics within 6 months of surgery
renal impairment, peptic ulcer disease, GI bleeding.

What this trial measures

  • Pain ScorePain scores will be recorded daily for the first 2 weeks, and then once a week until the 6 week post operative clinic visit.

    Analog pain score 0-10. A pain score of 10 represents maximum pain and a pain score of 0 represents no pain.