MedPath

A comparative study between combined adductor canal and infiltration of the interspace between popliteal artery and the capsule of posterior knee blocks versus combined adductor canal and periarticular injection blocks after total knee arthroplasty

Phase 4
Conditions
Anaesthesia
Registration Number
PACTR202306652234255
Lead Sponsor
faculty of medicine Ain Shams university
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

oAge group: less than 75 years old.
oSex: both sexes.
oASA I, II, III.
oType of anesthesia: Single shot spinal anesthesia.

Exclusion Criteria

oPatients’ refusal.
oHypersensitivity to Local anesthetics.
oBleeding tendency.
oLocal infection at site if injection.
oType of anesthesia: General anesthesia.
oASA IV.
oPrevious neuropathy on the operative limb

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain scores using VAS will be monitored 2 hourly for 24 hours and then 4 hourly for next 24 hours.
Secondary Outcome Measures
NameTimeMethod
Time for first rescue analgesia and total dose of rescue analgesia during first 48 hours postoperatively. <br>;Assessment of quadriceps muscle weakness by assessing patient’s ability to actively extend the knee and flex the hip.
© Copyright 2025. All Rights Reserved by MedPath