Analgesic Efficacy of Blocking Nerve to Vastus Lateralis Muscle Versus Lateral Femoral Cutaneous Nerve After Knee Surgeries

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKafrelsheikh University

About this trial

This study aims to compare the analgesic efficacy and functional outcomes of blocking the nerve to the vastus lateralis (NVL) muscle versus the lateral femoral cutaneous nerve (LFCN).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years.

Both sexes.

American Society of Anesthesiologists (ASA) physical status from I to III.

Underwent knee surgeries under spinal anesthesia.

Disqualifiers

Pregnancy.

Coagulopathy.

Neuromuscular disorders.

Hematological disorders.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Vastus lateralis nerve block

    Drug

    Patients received vastus lateralis nerve block with 5 ml of bupivacaine 0.5%.

  • Lateral femoral cutaneous nerve block

    Drug

    Patients received lateral femoral cutaneous nerve block with 5 ml of bupivacaine 0.5%.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Vastus lateralis nerve block groupExperimental treatment 1 intervention
Group B: Lateral femoral cutaneous nerve block groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Degree of pain

Each patient will be instructed about postoperative pain assessment using the numeric rating scale (NRS) score (0 represents "no pain" while 10 represents "the worst pain imaginable"). NRS assessments will be conducted at the post-anesthesia care unit (PACU) and at 2, 4, 6, 12, 18, and 24 hours postoperatively.

Time frame
24 hours postoperatively

Secondary outcomes

1

Time to first request for analgesia

The time to first request for analgesia will be recorded from the end of surgery till the first dose of morphine is administered.

Time frame
24 hours postoperatively
2

Total morphine consumption

If the numeric rating scale (NRS) exceeded 3, rescue analgesia in the form of a 3 mg morphine bolus will be administered, to be repeated after 30 minutes if the pain persisted until the NRS dropped below 4.

Time frame
24 hours postoperatively
3

Block performance time

The block performance time will be recorded from the placement of the ultrasound probe to the removal of the needle after the injection of local anaesthetic.

Time frame
Intraoperatively
4

Degree of patient satisfaction

The degree of patient satisfaction will be measured using a 5-point Likert scale (1 = extremely dissatisfied, 2 = unsatisfied, 3 = neutral, 4 = satisfied, 5 = extremely satisfied).

Time frame
24 hours postoperatively

Other outcomes

Sponsors and contacts

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