Supra Inguinal Fascia Iliaca Block Versus Ultrasound-guided Caudal Analgesia for Pediatrics Undergoing Anterior and Lateral Thigh Surgeries: A Randomized Controlled Trial

ConditionCancer Bone
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-18
SponsorNational Cancer Institute, Egypt

About this trial

patients will then be randomized in the two groups.

1. Group C: in this group children will receive US-guided caudal analgesia (CA) after GA. The caudal block will be performed 2. Group B: in this group children will receive lower limb peripheral nerve blocks in the form of US-guided fascia iliaca Block.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 1-12 years

scheduled for anterior and lateral thigh Surgeries

American Society of Anesthesiologists (ASA) physical status II or III

Disqualifiers

Refusal of parental consent

Allergy to any local anesthetics

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fascia Iliaca Nerve Block

    Other intervention

    With the patient in the proper position, the skin is disinfected and the transducer positioned to identify the femoral artery and the iliopsoas muscle and fascia iliaca. The transducer is moved laterally until the sartorius muscle is identified. After a skin wheal is made, the needle is inserted in-plane

  • Caudal Block Anesthesia

    Other intervention

    The caudal block will be performed by visualizing the sacral hiatus at the level of the sacral cornu after placing the probe transversely obtaining a short axis view, two hyperechoic lines will appear between the sacral cornu the superficial line is the sacrococcygeal ligament

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Group C: in this group children will receive US-guided caudal analgesia (CA) after GA.Active comparator 1 intervention
Group B: Group B: in this group children will receive lower limb peripheral nerve blocks in the form of USExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

• Estimation of time of first rescue postoperative analgesia

Time frame
4 hours postoperatively

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: