Actively Recruiting

Phase Not Applicable
Age: 21Years - 65Years
All Genders
NCT06802419

Effect of Continuous Adductor Canal Block Versus Continuous Adductor Canal Block With Additional Infiltration Between The Popliteal Artery and Capsule of The Knee (IPACK) After Arthroscopic Knee Surgeries

Led by Ain Shams University · Updated on 2025-01-31

70

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effect of Continuous Adductor Canal Block only versus adding posterior knee block, known as the Infiltration between the Popliteal Artery and Capsule of the Knee (IPACK) block with Continuous Adductor Canal Block (CACB) after arthroscopic knee surgeries.

CONDITIONS

Official Title

Effect of Continuous Adductor Canal Block Versus Continuous Adductor Canal Block With Additional Infiltration Between The Popliteal Artery and Capsule of The Knee (IPACK) After Arthroscopic Knee Surgeries

Who Can Participate

Age: 21Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 21 to 65 years
  • Both sexes
  • American Society of Anesthesiologists (ASA) Physical Status Class I to II
  • Patients with successful spinal anesthesia
  • Patients scheduled for elective arthroscopic knee surgery for anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) repair
Not Eligible

You will not qualify if you...

  • Declining to give written informed consent
  • History of allergy to the medications used in the study
  • Contraindications to regional anesthesia including coagulopathy and local infection
  • Polytrauma patients having lower limb fractures
  • Patients with pre-existing myopathy or neuropathy on the operating limb
  • Patients with diabetes mellitus
  • Psychiatric disorder
  • Morbid obesity (body mass index > 45kg/m2)
  • Complicated surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ain Shams University

Cairo, Egypt, 11591

Actively Recruiting

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Research Team

N

Nada E Hussein, Master

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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