A Comparison Between The Analgesic Efficacy of Adductor Canal Block Alone and Adductor Canal With IPACK (Interspace Between Popliteal Artery and Capsule of the Knee) Block for Knee Surgeries

Nerve Blocks Clinical Trial

Official title:

A Comparison Between The Analgesic Efficacy of Adductor Canal Block Alone and Adductor Canal With IPACK (Interspace Between Popliteal Artery and Capsule of the Knee) Block for Knee Surgeries

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT04995861
• Other study ID #: AinShamsU Shabayek MD
• Status: Enrolling by invitation
• Phase: N/A
• Start date: April 20, 2021
• Est. completion date: September 30, 2022

Study information

• Verified date: July 2022
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A comparison between The analgesic efficacy of adductor canal block alone and adductor canal with IPACK (interspace between popliteal artery and capsule of the knee) block for knee surgeries

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 50
• Est. completion date: September 30, 2022
• Est. primary completion date: September 20, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 70 Years

Eligibility

Inclusion Criteria:

• patients undergoing knee surgery i.e. arthroscopy, total knee replacement, ACL repair.

• ASA physical status I to III

• Sex (males and females)

• Age 21-70 years.

Exclusion Criteria:

• Hypersensitivity to local anesthetics. Preexisting peripheral neuropathy. Infection near site of infections e.g. osteomyelitis, septic knee joint. Etc. Patient refusal. PAny contraindications for spinal anesthesia. ( eg: coagulopathy, use of anticoagulants

Related Conditions & MeSH terms

• Nerve Blocks

Intervention

Procedure:
• Adductor canal block and IPACK block
Peripheral nerve blocks

Locations

Country	Name	City	State
Egypt	Ain Shams University	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of post operative pain	Using visual analogue scale (VAS) (scale 0-10, where 0 = no pain and 10 = worst imaginable pain)	One year
Secondary	Range of movement and ambulation	the range of movement (ROM) by assessing the degree of knee extension one day after the surgery, and ambulation distance assessed by the number of steps walked by the patient three days after the surgery.	One year