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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Adductor Canal Block (ACB) + iPACK Block

    Drug

    Patients who underwent total knee arthroplasty surgery with IPACK + adductor canal block , 25 patients. After the needle tip is placed in the target area between the popliteal artery and the femur, the local anesthetic solution (10 ml of 0.5% bupivacaine + 10 ml of physiological saline) is slowly injected after negative aspiration. After the needle tip is placed within the adductor canal, the local anesthetic solution (10 ml of 0.5% bupivacaine + 10 ml of physiological saline) is slowly injected after negative aspiration.

  • adductor canal block + genicular blocks

    Drug

    Patients who underwent total knee arthroplasty surgery with genicular blocks + adductor canal block , 25 patients. The tip of the needle is directed toward the superior lateral, superior medial, and inferior medial genicular nerves under ultrasound guidance.2 ml of local anesthetic (0.5% bupivacaine) is injected into each nerve region. After the needle tip is placed into the adductor canal, the local anesthetic solution (10 ml of 0.5% bupivacaine + 10 ml of physiological saline) is slowly injected after negative aspiration.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: GROUP IPACKOther 1 intervention
Group B: GROUP GENİCULARExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

6-Clicks score

Known as "6-Clicks" due to being composed of six scored patient activity questions, a patient's "6-Clicks" score falls on a 6- to 24-point scale where a score of 6 represents total functional impairment and a score of 24 represents total absence of impairment.

Time frame
6.,12.,24.,36.,48.,60.,72. hours

Secondary outcomes

1

visual analog scale

The Visual Analogue Scale (VAS) is a psychometric instrument used in research and clinical studies to measure the intensity of subjective experiences that cannot be objectively quantified using defined biomarkers, such as pain, fatigue, or mood. It typically consists of a 100 mm straight line with descriptive anchors at each end representing the extremes of the sensation (for example, "no pain" at one end and "the most severe pain imaginable" at the other).

Time frame
Postoperative recovery room 30 minutes and at 6., 12., 24., 36., 48., 60., and 72. hours
2

total opioid consumption

total opioid consumption per day

Time frame
total opioid consumption 24.hour
3

The Patient Satisfaction Index

The Patient Satisfaction Index (PSI) was used to describe self-evaluation of the outcome and responseof 1 or 2 was considered to indicate a satisfying outcomeand 3 or 4 to indicate a dissatisfied outcome.

Time frame
first 24. hour

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: