Postoperative Analgesic Efficacy Between Adductor Canal Block + IPACK Block and Adductor Canal Block + Genicular Nerve Block in Total Knee Arthroplasty

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKonya Beyhekim Training and Research Hospital

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

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

This trial has no locations