About this trial
The aim of this study is to compare the postoperative analgesic efficacy and functional outcomes of the IPACK+Adductor Canal Block with the Genicular Nerve Block+Adductor Canal Block block in patients undergoing total knee arthroplasty (TKA). The primary objective (measurable) is to evaluate functional improvement using 6-Clicks scores, while secondary objectives include pain scores (Vas Score), opioid consumption, hospital stay duration, and patient satisfaction (Patient Satisfaction Index).
IPACK : The infiltration between the popliteal artery and capsule of the knee
Eligibility criteria
Qualifiers
Patients scheduled for spinal anesthesia with TDA.
Age ≥18.
American Society of Anesthesiologists (ASA) physical status score I-III.
Patients capable of providing informed consent.
Disqualifiers
Active infection at the injection site.
Coagulopathy or systemic sepsis.
Severe hypovolemia.
Patients who refuse regional anesthesia.
Trial design
Treatments tested in this trial
- Adductor Canal Block (ACB) + iPACK Block
- adductor canal block + genicular blocks