Clinical Trial

Clinical Practice of Hydromorphone in Multimodal Analgesia for Enhanced Recovery After Surgery (ERAS) in Knee Arthroplasty

Completed
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Summary
This study proposes a multimodal analgesia regimen comprising preoperative non-steroidal anti-inflammatory drugs (NSAIDs) for preemptive analgesia, intra-articular injection at the end of surgery, and postoperative adductor canal block. The objective is to observe the analgesic efficacy and duration of hydromorphone combined with ropivacaine in the adductor canal block on resting and movement-related pain in patients following total knee arthroplasty, as well as the time to recovery from motor blockade and the incidence of drug-related adverse events.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-20.
Trial Details
NCT Number NCT07722234
Lead Sponsor China-Japan Friendship Hospital
Conditions VAS Score, Quadriceps Strength
Enrollment 90 participants
Start Date 2026-03-10
Primary Completion 2026-06-10 (estimated)
Study Completion 2026-06-13 (estimated)
Updated on ClinicalTrials.gov 2026-07-27