Postoperative Analgesic Efficacy of ACB+iPACK vs FTB+Selective Tibial+Obturator Blocks in ACL Reconstruction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16+
SponsorDa Nang Hospital

About this trial

This prospective, comparative study aims to evaluate the postoperative analgesic efficacy of ultrasound-guided Adductor Canal Block (ACB) combined with iPACK block versus Femoral Triangle Block (FTB) combined with selective tibial nerve block and obturator nerve block in patients undergoing arthroscopic anterior cruciate ligament (ACL) reconstruction. The primary objective is to determine which regional anesthesia regimen provides superior pain relief at rest and during movement. The secondary objectives include assessing morphine consumption, motor blockade using the Bromage score, patient satisfaction, and potential adverse effects of these anesthesia techniques.

Eligibility criteria

Qualifiers

Age 16 years and older

Patients undergoing elective arthroscopic anterior cruciate ligament (ACL) reconstruction

ASA physical status I-II

Indicated for spinal anesthesia

Disqualifiers

Infection at the injection site

Spinal cord or lower limb nerve injury

Contraindications to regional anesthesia (Levobupivacaine)

Known allergy to Paracetamol or Diclofenac

Trial design

Treatments tested in this trial

  • Ultrasound-guided Adductor Canal Block (ACB)
  • Ultrasound-guided iPACK block
  • Ultrasound-guided Femoral Triangle Block (FTB)
  • Ultrasound-guided Selective Tibial Nerve Block
  • Ultrasound-guided Obturator Nerve Block

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators