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Anterior Cutaneus Nerve and Distal Adductor Canal Block With USG for Total Knee Replacement Analgesia

D

Diskapi Teaching and Research Hospital

Status

Completed

Conditions

Knee Replacement Arthroplasty
Nerve Block
Pain Measurement

Treatments

Procedure: Distal adductor canala blockade and anterior cutaneus nerve blockade
Procedure: Adductor canal blockade

Study type

Interventional

Funder types

Other

Identifiers

NCT06201195
AEŞH-EK1-2023-556

Details and patient eligibility

About

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?

Full 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.

Enrollment

58 patients

Sex

All

Ages

40 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Total knee artroplasty
  • Spinal anesthesia
  • ASA 1-3

Exclusion criteria

  • Bupivacaine allergy
  • Coagulopathy
  • Infection on injection site

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

58 participants in 2 patient groups

Adductor canal block
Active Comparator group
Description:
Usg guidance adductor canal block with %0.25 Bupivacaine 20 ml
Treatment:
Procedure: Adductor canal blockade
Distal adductor canal block with anterior cutaneus nerve block
Active Comparator group
Description:
Usg guidance distal adductor canal block (%0.25 Bupivacaine 20 ml) with anterior cutaneus nerve block (%0.25 Bupivacaine 10 ml)
Treatment:
Procedure: Distal adductor canala blockade and anterior cutaneus nerve blockade

Trial contacts and locations

1

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Central trial contact

Derya Ozkan, professor MD

Data sourced from clinicaltrials.gov

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