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Study identifier: NCT06600815 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Analgesic Efficacy of Preemptive Stepwise Infiltration Anesthesia for Perioperative Analgesia After TKA

Condition: Total Knee Arthroplasty · Pain Management  ·  Sponsor: First Affiliated Hospital of Fujian Medical University

PhaseNA
Planned participants110
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

This is a single-center prospective cohort study in which patients were evaluated by inclusion and exclusion criteria before total knee arthroplasty (TKA). Eligible patients will be included in this study after signing the informed consent form. Before TKA, the patients will be randomly assigned to either a preemptive stepwise infiltration anaesthesia (PSIA) group or a postoperative local infiltration analgesia (PLIA) group and administered different pain management protocols during surgery. Clinical evaluation will be conducted at baseline, before surgery, and at 6, 12, 24, 48, and 72 hours postoperatively, as well as during follow-up visits at 3 weeks, 6 weeks and 6 months postoperatively. All patients voluntarily participated in the study and signed informed consent. During the treatment period, all prospective patients underwent clinical evaluation at the end of total knee arthroplasty and 6, 12, 24, 48, 72, and 96 weeks later, aimed at comparing the postoperative pain and inflammatory response between PSIA and PLIA, to explore the optimal perioperative analgesic modality for TKA.

This description comes directly from the study's public registry record.

Talk to the study team

Xinyu Fang, MD  ·  18084768503 Ext. 86  ·  9738006@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital of Fujian Medical UniversityFuzhou, Fujian, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06600815