Opioid-Free Pain Treatment in Trauma Patients
Public ClinicalTrials.gov record NCT06078371. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Peri-operative Opioid-free Analgesic Protocol for Orthopedic Trauma Patients
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Analgesic drug study that will compare pain outcomes of opioid analgesia and opioid-free analgesia in post-operative orthopedic patients.
Study identification
- NCT ID
- NCT06078371
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 250 participants
Conditions and interventions
Conditions
- Femoral Neck Fractures
- Intertrochanteric Fractures
- Femoral Shaft Fracture
- Distal Femur Fracture
- Patella Fracture
- Tibial Shaft Fracture with or Without Associated Fibula Fracture
- Ankle Fracture (bimalleolar Equivalent, Bimalleolar, or Trimalleolar)
- Tibial Pilon Fracture
- Talar Head, Neck, Body, or Process Fractures
- Calcaneus Fractures
- Lisfranc Injuries
- Isolated or Multiple Metatarsal Fractures
- Phalanx Fractures of the Foot, Single or Multiple
- Clavicle Fractures
- Proximal Humerus Fractures
- Humeral Shaft Fractures
- Distal Humerus Fractures (intra or Extra-articular)
- Olecranon Fractures
- Radial Head or Neck Fractures
- Elbow Fractures Involving a Combination of Fractures of the Radius and Uln
- Forearm Fractures (both Bone Forearm Fractures, Isolated Ulnar Shaft, Isolated Radial Shaft)
- Distal Radius Fractures
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Oct 31, 2023
- Primary completion
- Sep 30, 2026
- Completion
- Sep 30, 2026
- Last update posted
- Oct 25, 2024
2023 – 2026
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| The University of Kansas Medical Center | Kansas City | Kansas | 66103 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06078371, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 25, 2024 · Synced Sep 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06078371 live on ClinicalTrials.gov.