Erector Spinae Plane Block Versus Quadratus Lumborum Block

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age2-12
SponsorAssiut University

About this trial

To compare the efficacy and safety of ultrasound-guided ESPB versus QLB for post-operative analgesia in children undergoing kidney surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Infection at the site of needle insertion

Allergy to local anesthetics

Parental refusal of consent

Trial design

Design model

Parallel

Treatments tested in this trial

  • Quadratus lumborum block teqnique

    Procedure/Surgery

    All blocks were performed under ultrasound guidance. A high-frequency linear probe was positioned in the mid-axillary line cranial to the iliac crest to identify the abdominal wall muscles (external oblique, internal oblique, and transversus abdominis). The probe was then moved dorsally until the transversus abdominis muscle became aponeurotic, which was followed medially to visualize the quadratus lumborum (QL) muscle at its attachment to the L4 transverse process adjacent to the psoas muscle. Using an in-plane anterior-to-posterior approach, the block needle was advanced toward the anterior border of the QL muscle. After confirming the needle tip position with a 1 ml saline test injection, 0.5 ml/kg of 0.25% bupivacaine was administered. Bilateral injections were performed for midline incisions, while unilateral injections were used for paramedian incisions.

  • Erector spinae plane block Technique

    Procedure/Surgery

    Ultrasound-guided erector spinae plane block performed at the thoracic level using a single-shot technique in pediatric patients undergoing kidney surgery to provide postoperative analgesia. Local anesthetic is injected deep to the erector spinae muscle over the transverse process with expected craniocaudal spread.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Erector spinae plane blockExperimental treatment 2 interventions
Group B: Quadratus lumborum blockActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Time to first rescue analgesia

measured from extubation until the first request/administration of analgesia, in hours

Time frame
24 hours

Secondary outcomes

1

Total analgesic consumption

Total 24-hour postoperative analgesic consumption (mg/kg paracetamol, µg/kg fentanyl).

Time frame
24 hours
2

Postoperative pain score

FLACC pain score assessed at 0, 1, 2, 6, 12, and 24 hours postoperatively.

Time frame
24 hours
3

Incidence of postoperative nausea and vomiting

Incidence of PONV within 24 hours postoperatively.

Time frame
24 hours
4

Block-related complications

Incidence of block-related complications.

Time frame
24 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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