Adductor Canal Block plus IPACK Block vs Isolated Adductor Canal Block for Postoperative Analgesia in ACLR with Bone Patellar Tendon Bone Autograft

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Anterior Cruciate Ligament Rupture
  • Age: Between 18 years - 75 years
  • Gender: Male or Female
  • Other Inclusion Criteria:
    1. Patients undergoing primary anterior cruciate ligament (ACL) reconstruction with Bone Patellar Tendon Bone (BPTB) Autograft
    2. Adductor Canal Block (ASA) I or II

You may not be eligible for this study if the following are true:

    1. Participants with multi-ligament injury
    2. Participants undergoing concomitant cartilage procedure or osteotomy
    3. Participants with a history of chronic pain that have used opioids for pain management for 3 months or longer
    4. Participants who are allergic to oxycodone
    5. Participants with diagnosed or self-reported cognitive dysfunction
    6. Participants with a history of neurologic disorder that can interfere with pain sensation
    7. Participants with a history of drug or recorded alcohol abuse
    8. Participants who are unable to understand or follow instructions
    9. Participants with severe liver disease, renal insufficiency, congestive heart failure, and/or significant heart disease
    10. Participants with an allergy or contraindication to any of the medications used in the study, or patients with a contraindication to any study procedures
    11. Participants with a BMI over 45
    12. Any participant that the investigators feel cannot comply with all study related procedures
    13. Any pregnant participant; assessed via urine pregnancy test in the preoperative area as part of standard preoperative surgical protocol

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.