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Efficacy of an AFCN Proxy Block in Post-TKA Multimodal Pain Management

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary endpoint(s) modifiedv4 Show 8 more changesShow less
    • Start date: Jun 2026 to Aug 1, 2026
    • Primary completion pushed from Jun 2027 to Aug 1, 2027
    • Study completion pushed from Jul 2027 to Sep 1, 2027
    • Study sites: 0 to 1
    • Secondary endpoints: 5 to 6
    • Study description expanded, about 67 words
    • Publications: 5 to 6
    • Study title expanded, about 1 word
  2. Start date: Jan 2026 to Jun 2026
    • Primary completion date: Jan 2027 to Jun 2027
    • Study completion date: Feb 2027 to Jul 2027
    v3
  3. Re-verified, no change to tracked fieldsv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This randomized controlled trial evaluates the additive effect of Supra-Sartorial Subcutaneous Infiltration (SSSI) when performed in combination with intermittent adductor canal block (iACB) and posterior capsule local infiltration analgesia (PC-LIA) for pain management after total knee arthroplasty (TKA). SSSI, an easy-to-perform tentative proxy block to targeted anterior femoral cutaneous nerve (AFCN) block, is tested in 90 adults (45-90 years) randomized into two arms: active SSSI versus sham SSSI. Primary outcome is pain scores at rest and during movement on postoperative day 0; secondary outcomes include daily pain trajectory at rest and during movement, functional recovery scores, rescue analgesic doses over days 0-3, and quality of recovery assessment on day 4.
Trial Details
NCT Number NCT07191964
Lead Sponsor Taipei Medical University WanFang Hospital
Conditions
(from sponsor)		 Postoperative Pain Management in Total Knee Arthroplasty
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov