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Pericapsular Nerve Group Block Versus Caudal Block for Postoperative Pain Management in Pediatric Hip Surgery

Ultrasound-Guided Pericapsular Nerve Group Block Versus Ultrasound-Guided Caudal Block for Postoperative Pain Management in Pediatric Hip Surgery; a Randomized Controlled Trail

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06563622
Enrollment
80
Registered
2024-08-21
Start date
2024-08-10
Completion date
2025-04-20
Last updated
2025-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Postoperative

Brief summary

Children can experience substantial pain after hip operations, causing agitation, depression, and sleep disruption, which can have a negative impact on their health. Opioids are associated with several serious side effects that limits its use as solo agents for pain management. Regional blocks such as caudal Block (CB) and pericapsular nerve group (PENG) block in adjuvant with general anaesthesia are alternative perioperative analgesic techniques that lead to lesser side effects, including motor weakness, postoperative nausea and vomiting with decreased opioid consumption.

Detailed description

Regional anesthesia is often used to prevent postoperative pain in pediatric surgery. Combined with general anesthesia (GA), ultrasound (US)-guided regional anesthetic approaches provide simple intraoperative pathway that reduced GA requirements, lower pain score with less impact on the respiratory or cardiovascular system In pediatric surgery, caudal block (CB) is a low-cost, simple, and effective procedure for postoperative analgesia. CB is suggested for most surgeries in the lower body, primarily below the umbilicus. Although the well-established anesthetic properties of CB, its action terminates early in the postoperative period and it has a number of restrictions, such as anatomical abnormalities or infection at the injection site, that can prevent its use PENG block is the plane lying between the psoas muscle and tendon and the ilio-pubic eminence. The single-shot PENG block has lately been reported in the cadaveric study and in the literature for perioperative pain management in hip surgery by aiming the articular arms of the accessory obturator nerve (AON), femoral nerve (FN), and obturator nerve (ON). The technical simplicity of imaging in traction-fixed patients and no need for multiple punctures made this blockage ideal for young pediatric patients. Unfortunately, there are no adequate studies regarding PENG block in patients younger than five years old. This study was carried out to assess ultrasound-guided PENG block versus CB for their efficacy, safety and pain management in pediatric hip surgery.

Interventions

PROCEDUREPericapsular Nerves Group Block

USG-guided single-shot PENG in a dose of 0.5 ml/kg of 0.25% bupivacaine per side.

USG-guided single-shot CEB in a dose of 0.5 mL/kg of 0.25% bupivacaine.

Sponsors

Benha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

* child aged 1- 7 years old * American Society of Anesthesiologists (ASA) physical status I-II * scheduled for elective hip surgery under general anesthesia

Exclusion criteria

* parents/guardians refusal to participate * known local anesthetic drug sensitivity, * bleeding disorders, * pre-existing infection at the block site, and * the presence of major cardiac, renal, or hepatic disorders.

Design outcomes

Primary

MeasureTime frameDescription
pain score with FLACC30 minutes postoperative, 1 hour postoperative, 2 hour postoperative, and 6 hours postoperative(Face, Legs, Activity, Cry, and Consolability scale to assess pain in young children. Each category is scored on a 0-2 scale which results in a total score between 0 (lowest pain) and 10 (worst pain).

Secondary

MeasureTime frameDescription
The duration of the blockimmediately after the intervention, up to 24 hours postoperativefrom immediately after the block administration until the first postoperative rescue analgesia.
the Time to first postoperative rescue analgesia24 hours postoperativeit will be administered if the FLACC score is ≥ 4/10.
Total rescue analgesia consumption24 hours postoperativetotal dose of Morphine administrated as rescue opioid
The incidence of postoperative adverse effects24 hours postoperativeincluding nausea , vomiting , localized hematoma, bradycardia, hypo-tension, and Pruritis.
Parents satisfaction score24 hours postoperativeusing a 5- point Likert score (0 = very dissatisfied, 1=dissatisfied, 2 = neither satisfied nor dissatisfied, 3 = satisfied and 4 = very satisfied)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026