Contribution of Anterior Femoral Cutaneous Nerve Block to Postoperative Analgesia for Total Knee Replacement
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pain Measurement
- Sponsor
- Diskapi Teaching and Research Hospital
- Enrollment
- 58
- Locations
- 1
- Primary Endpoint
- drain place pain
- Status
- Completed
- Last Updated
- 5 months ago
Overview
Brief Summary
This prospective clinical study was approved by the institutional ethics committee on September 27, 2023, and patient enrollment started in October 2023. the study aimed to evaluate the contribution of anterior femoral cutaneus nerve block to postoperative analgesia in total knee artroplasty.
The goal of this clinical trial is to compare analhesia effects of adductor canal blockade versus distal adductur canal blockade added anterior cutaneus nerve block in total knee arthroplasty.
The main questions it aims to answer are:
- question 1: does distal adductor canal blockade + anterior cutaneus nerve blokade superior analgesia then adductor canal block for undergoing TKP?
- question 2: does distal adductor canal blockade + anterior cutaneus nerve blokade decrease drain place pain on anterolateral face of knee?
Detailed Description
Patients with American Society of Anesthesiologists classification status I-III scheduled for elective primary TKA using standard spinal anesthesia enroll for this trial. After surgery patient divided two groups: 1- adductor canal blockade 2- distal adductor canal blockade + anterior femoral cutaneus nerve blockade. At postoperative 3th, 10th, 24th hour VAS (visuel analouge scale), VAS move, incision plase pain-for top and down of patella, drain place pain, motor strenght for femoral nerve and siyatic nerve, first analjesic requirement time, opioid consumption, total analcesic requirement will be recorded.
Investigators
derya özkan
professor
Diskapi Teaching and Research Hospital
Eligibility Criteria
Inclusion Criteria
- •Total knee artroplasty
- •Spinal anesthesia
Exclusion Criteria
- •Bupivacaine allergy
- •Coagulopathy
- •Infection on injection site
Outcomes
Primary Outcomes
drain place pain
Time Frame: postblock 3 hour,10 hour, 24 hour
do you have any pain on drain place? yes or no
VAS (visuel analouge scale)
Time Frame: postblock 3 hour,10 hour, 24 hour
for postoperative pain evaluation after TKA surgery. The visual analogue scale (VAS) uses a 10 cm line with endpoint descriptors such as 'no pain' marked at the left end of the line and 'worst pain imaginable' marked at the right end.
Secondary Outcomes
- motor strenght(postblock 3 hour,10 hour, 24 hour)
- VAS movement(postblock 3 hour,10 hour, 24 hour)