Block and Periarticular Injection Study - Trial NCT06410612
Access comprehensive clinical trial information for NCT06410612 through Pure Global AI's free database. This Phase 4 trial is sponsored by Washington University School of Medicine and is currently Enrolling by invitation. The study focuses on Pain, Postoperative. Target enrollment is 200 participants.
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Study Focus
Sponsor & Location
Washington University School of Medicine
Timeline & Enrollment
Phase 4
Mar 04, 2024
Mar 01, 2025
Primary Outcome
Mean Visual Analog Scale (VAS) pain score for 2 weeks postoperatively
Summary
The purpose of the study is to compare two types of perioperative analgesic modalities,
 adductor canal block plus interspace between popliteal artery and capsule of the knee (IPACK)
 block and periarticular injection versus periarticular injection alone, to determine their
 relative efficacies with regard to pain relief and functional outcomes in the early
 postoperative period following primary total knee arthroplasty.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06410612
Non-Device Trial