Post Operative Pain
Conditions
Brief summary
The purpose of this study is to evaluate the effectiveness and safety of tramadol and oxycodone therapy in comparison to oxycodone alone as part of a multimodal pain regimen to reduce postoperative opioid consumption, pain, minimize adverse events and complications for primary total knee arthroplasty (TKA) and primary total hip arthroplasty (THA).
Interventions
DRUGOxycodone
Patients will receive oral Oxycodone only to treat post-operative pain: Oxycodone 5mg * Patients ≤75 years old: 5mg or 10 mg PO every 4 hr as needed * 5 mg for pain rated 4-6 * 10 mg for pain rated 7-10 * Patients \>75 years old and/or sensitive to opioids or sedatives: 2.5mg or 5mg every 4hr as needed * 2.5mg for pain rated 4-6 * 5mg for pain rated 7-10
DRUGTramadol and Oxycodone
Patients will receive a combination of Tramadol and Oxycodone to take orally to treat post-operative pain: Tramadol 50mg * Patients ≤75 years old: 50 mg for pain rated 4-6; 100 mg for pain rated 7-10 * Patients \>75 years old and/or sensitive to opioids or sedatives; use 50 mg * Dosing is every 8 hours as needed. Cumulative dose not to exceed 400mg in 24 hours Oxycodone 5mg * Patients ≤75 years old: 5mg or 10 mg PO every 4 hr as needed if still having pain after maximum tramadol administration * 5 mg for pain rated 4-6 * 10 mg for pain rated 7-10 * Patients \>75 years old and/or sensitive to opioids or sedatives: 2.5mg or 5mg every 4 hr as needed if still having pain after maximum tramadol administration * 2.5 mg for pain rated 4-6 * 5 mg for pain rated 7-10
Sponsors
Mayo Clinic
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Primary TKA * Primary THA * Age \> 18 years
Exclusion criteria
* Age \< 18 years * Revision or partial TKA/THA * Pregnant or breast-feeding women * Simultaneous bilateral TKA/THA * Primary TKA/THA due to oncologic reason * Anaphylaxis to opioids * Renal or liver failure * Prior opioid use disorder/ substance use disorder * Opioid use within 3 months prior to surgery * Patients needing a translator and those with dementia or other cognitive deficits * Patients taking Monoamine Oxidase Inhibitor (MOAI) medications (phenelzine, tranylcypromine) or benzodiazepine medications (alprazolam, diazepam, lorazepam, etc)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cumulative opioid consumption during the first 30 days | 30 days | Total amount of opioid medication taken for the first 30 days following surgery, reported in milligrams (mg) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Cumulative opioid consumption during the first 90 days | 90 days | Total amount of opioid medication taken for the first 90 days following surgery, reported in milligrams (mg) |
| Postoperative opioid refills within 90 days | 90 days | Total number of opioid medication refills within 90 days post surgery |
| Number of unused opioid pills | 90 days | Total number of unused opioid pills unused after 90 days |
| Change in Visual Analogue Scale (VAS) pain scores | Daily for 90 days | Pain values reported by participants will be assessed using the 100-mm Visual Analogue Scale (VAS). The VAS line will be 100 mm long with no intermediate delineations. Each end will be marked with "no pain" on the left, and "worst possible pain" on the right. Participants will identify their pain level by indicating a point on the line between each end. That point will be measured from the "No pain" end, and the number of millimeters will be reported as the pain score. |
| Number of complications | 90 days | Total number of complications experienced post-operatively, complications include stiffness, VTE, GI hemorrhage, falls, ileus, dizziness, changes in vision, and miosis. |
| Number of emesis episodes | 90 days | Postoperative nausea and vomiting will be measured by total number of emesis episodes |
| Rate of antiemetic use | 90 days | Total number of times patients require use of antiemetics for nausea or vomiting |
| Satisfaction survey scores | 90 days | Patients will be provided with a satisfaction survey 90 days post-surgery. The survey consists of 2 questions rated on a Likert scale measuring understanding and confidence in medication use, and one yes/no question. The Likert scale questions are ranked from "0" - no understanding/low confidence to "10" - full understanding/high confidence. Higher scores indicate greater satisfaction with the prescribed opioid therapy plan. |
| Length of Stay | Post-operatively, up to 90 days | Total number of days patients stay inpatient |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORCharles P. Hannon, MD, MBA
Mayo Clinic
Outcome results
None listed