Enhanced Recovery After Surgery (ERAS) Total Knee Replacement (TKR) With a Transitional Pain Service
This study is comparing two different methods of pain control for total knee replacement surgery in adults aged 18 to 65. Both methods involve a combination of pain relief techniques, but they differ in how one specific pain block, called an adductor canal block (ACB), is delivered. One group will receive a single shot of the ACB, while the other will receive a continuous adductor canal catheter (ACC) which delivers pain medicine over time. Researchers want to see which method leads to less opioid pain medication use in the first 24-48 hours after surgery. You may be eligible if you have osteoarthritis, are scheduled for a total knee replacement, speak English, live within an hour of the hospital, and have a smartphone. The study's current status is unclear.
- Study design
- This is an interventional study where 94 participants will be randomly assigned to one of two groups to compare different pain management techniques.
- What's involved
- You would receive either a single-shot adductor canal block or a continuous adductor canal catheter as part of your pain management during and after total knee replacement surgery.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your opioid consumption will be measured for 24-48 hours after your spinal anesthesia.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Enhanced Recovery After Surgery (ERAS) Total Knee Replacement (TKR) With a Transitional Pain Service
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- David Kim, MD · PRINCIPAL_INVESTIGATOR · Hospital for Special Surgery, New York
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Opioid consumption during 24-48 hour periodPost-operative day 1-2 (24-48 hours post spinal induction)
Patients will be asked to report their opioid consumption during the 24-48 hour time period after spinal induction. This data will be converted to morphine milligram equivalents (mme).