Effect of Posterior Femoral Cutaneous Nerve Block on Postoperative Posterior Lateral Knee Analgesia in Patients With TKA

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-80
SponsorGeneral Hospital of Ningxia Medical University

About this trial

The aim of this study was to observe the effects of posterior femoral cutaneous nerve block combined with sciatic and saphenous nerve block compared with sciatic and saphenous nerve block alone on postoperative posterior side of the knee (popliteal fossa) pain and sleep quality in patients with TKA, and to further alleviate postoperative posterior side of the knee pain in patients with TKA and improve the quality of postoperative sleep.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients who are >45 years of age; intended to undergo elective first TKA under general anesthesia

ASA grade II-III.

Agreed to participate in this study and signed the informed consent form.

BMI less than 28Kg/m2.

Disqualifiers

Patients who refuse to participate in the trial

Preoperative inability to communicate due to speech and hearing impairment, etc.

History of allergy to local anesthetics or opioids

Contraindications to nerve block operation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Posterior Femoral Cutaneous Nerve Combined With Proximal Sciatic and Saphenous Nerve Block

    Procedure/Surgery

    All nerve blocks were performed under ultrasound guidance,single supragluteal approach sciatic nerve block using a nerve stimulator, 20 ml of drug was injected around the sciatic nerve, the extent of drug diffusion was observed, the needle tip was turned into the deep surface of the gluteus maximus muscle below the deep gluteal artery and 5 ml of drug was injected, followed by a retractile canal saphenous nerve block injected with 15 ml of drug, and the difference in sensation of the posterior thighs of the bilateral thighs was measured after 15 min to ensure posterior femoral cutaneous nerve were blocked

  • Simple Sciatic and Saphenous Nerve Blocks

    Procedure/Surgery

    All nerve blocks were performed under ultrasound guidance,single subgluteal approach sciatic nerve block using a nerve stimulator, with 25 ml of drug injected around the sciatic nerve, followed by a retractile canal saphenous nerve block with 15 ml of drug injection

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: Sciatic saphenous nerve block group (Group S)Active comparator 1 intervention
Group B: Combined posterior femoral cutaneous nerve block group (Group P)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Postoperative anteroposterior and posterior knee Visual Analogue Scale scores (passive motion/resting)

The level of pain at the knee surface incision and on the posterior side of the knee at rest and motion was asked and recorded using the Visual Analogue Scale scores at postoperative hour 1 (before the patient left the PACU), postoperative hour 6, postoperative hour 24, and postoperative hour 48, respectively (0 for no pain and 10 for the most severe pain imaginable)

Time frame
postoperative hour 1,postoperative hour 6,postoperative hour 24,postoperative hour 48

Secondary outcomes

1

Postoperative night sleep time

Use of exercise bracelets to record actual hours of patient sleep

Time frame
First night after surgery, second night after surgery
2

Earliest time on the ground

Length of time between the end of surgery and the patient's active movement off the floor

Time frame
Within 48 hours of surgery
3

Amount of remedial opioid use

Total remedially applied opioids within 48 hours of surgery

Time frame
Within 48 hours of surgery
4

Number of patient PCNA uses

Number of times a patient presses the PCNA in the 48 hours postoperatively

Time frame
Within 48 hours of surgery

Other outcomes

Sponsors and contacts

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