Analgesic Comparison of PENG/LFCN to FICB for Total Hip Arthroplasty
Status unconfirmed · Not applicable
Conditions studied: Analgesia
In brief
This study compares 2 commonly used interventions (regional pain blocks) used in hip arthroplasty for pain control. One of the interventions is newer and not widely established.
Key facts
- Study ID
- NCT05477641
- Run by
- SSM Health Bone and Joint Hospital at St Anthony
- People needed
- 105
- Starts
- 2022-07-28
- Expected to finish
- 2023-02-01
- Last updated by the study team
- 2022-08-01
Who can join
Age: 40 and older, up to 80. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Eligibility criteria for the study were: age 40-80, Physical Status I-III, BMI less than 40 kg/m2, ability to read and speak English, able to sign their own consent form and undergoing elective primary total hip arthroplasty.
You may not qualify if…
- Patients were excluded if they were chronically prescribed opioids for a condition unrelated to their surgical hip pain, were deemed Physical Status 4 or higher, had an ongoing coagulopathy, had any infection near the site of injection, had an allergy to local anesthetics, deemed to have diabetic neuropathy, deemed to have a contraindication to spinal anesthesia or were unable to report their pain scores reliably (as in severe dementia or similar).
Where it is running
- SSM Healthcare Bone and Joint Hosptial at St Anthony — Oklahoma City, Oklahoma, United States (enrolling)
Full record on ClinicalTrials.gov
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