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Adductor Canal Block Combined With IPACK vs Genicular Nerves Block in Knee Arthroscopy

T

Tanta University

Status

Unknown

Conditions

Arthroscopy
Genicular Nerves Block

Treatments

Biological: Spinal anesthesia and ultrasound-guided Genicular nerves block
Procedure: Spinal anesthesia only
Biological: Ultrasound-guided Adductor Canal block (ACB) technique with infiltration of the interspace between popliteal artery and the capsule of posterior knee block ('PACK)

Study type

Interventional

Funder types

Other

Identifiers

NCT05269095
35236/1/22

Details and patient eligibility

About

This prospective randomized controlled study is designed to investigate the postoperative analgesic effect of adductor canal block (ACB) combined with infiltration of the interspace between the popliteal artery and the capsule of posterior knee (IPACK) block compared to genicular nerves block in patients undergoing knee arthroscopy.

Full description

Maintaining patient safety, ensuring best patient outcomes, and optimal pain relief post-operatively are of utmost concern for anesthesia providers. Adequate pain relief attenuates stress responses and long-term chronic pain complications while contributing to improved postoperative outcomes.

Knee arthroscopy is a very common procedure and very often is performed as day-case surgery. Ambulatory arthroscopic surgery of the knee is preferred by the majority of properly selected and well-informed patients. It has been reported that a significant number of patients have moderate to severe pain 24 hours after ambulatory surgery in general and knee arthroscopy in particular and pain affects the patient's activity level and satisfaction. Adductor canal block (ACB) is a popular peripheral nerve block that has been shown to decrease the pain significantly and decrease opioid consumption with minimal effect on quadriceps function. It provides analgesia to the peri-articular and intra-articular aspects of the knee joint but doesn't relieve posterior knee pain which is moderate to severe in intensity.

Enrollment

105 estimated patients

Sex

All

Ages

21 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 21-60 years
  • Both genders
  • American Society of Anaesthesiologists physical status classification I - III
  • Patients scheduled for elective unilateral knee arthroscopy under spinal anesthesia

Exclusion criteria

  • Patient refusal
  • Preoperative neurological deficits
  • Opioid-dependent (opioid intake more than 3 months)
  • Chronic pain conditions
  • Significant cardiac and respiratory disease
  • Pre-existing major organ dysfunction such as hepatic and renal failure
  • Coexisting hematological disorder or deranged coagulation parameters
  • Psychiatric illnesses
  • Allergy to any of the drugs used in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

105 participants in 3 patient groups

spinal anesthesia only
Experimental group
Description:
Patients will receive spinal anesthesia only
Treatment:
Procedure: Spinal anesthesia only
spinal anesthesia and ultrasound-guided Genicular nerves block
Experimental group
Description:
Patients will receive spinal anesthesia and ultrasound-guided Genicular nerves block
Treatment:
Biological: Spinal anesthesia and ultrasound-guided Genicular nerves block
Spinal anesthesia and US guided Adductor canal nerve block plus infiltration of the interspace
Experimental group
Description:
Patients will receive spinal anesthesia and ultrasound-guided Adductor canal nerve block plus infiltration of the interspace between the popliteal artery and the capsule of the posterior knee (PACK) block.
Treatment:
Biological: Ultrasound-guided Adductor Canal block (ACB) technique with infiltration of the interspace between popliteal artery and the capsule of posterior knee block ('PACK)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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