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Comparison of ultrasound guided placement of local anaesthetic in the abdominal muscle and local anaesthetic under the skin for pain relief during and following surgical repair of belly button hernias in children

A comparison of ultrasound-guided rectus sheath block and subcutaneous local anaesthetic infiltration for pain relief following paediatric umbilical hernia repair

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12608000488303
Enrollment
60
Registered
2008-09-30
Start date
2008-02-18
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

If the primary hypothesis is confirmed, this study will provide evidence supporting ultrasound placement of bilateral rectus sheath nerve blocks. At present subcutaneous periumbilical local infiltration is the community standard. No study has compared the two techniques to assess which method is more effective for providing analgesia for umbilical hernia repair in paediatric patients. The results of this study may show that ultrasound guided rectus sheath block provides more effective analgesia resulting in patients having decreased analgesic requirements following the periumbilical hernia repair.

Interventions

Anaesthesia and intraoperative management General anaesthesia will be induced with 1-8% sevoflurane via a facemask. Anaesthesia will be maintained with 1 minimum alveolar concentration (MAC) sevoflurane. Intraoperative monitoring will include pulse oximetry, non-invasive blood pressure, electrocardiogram (ECG), end tidal carbon dioxide concentration and heart rate. An intraoperative increase in respiratory rate, heart rate or mean arterial pressure of >20% following skin incision or during surg

Anaesthesia and intraoperative management General anaesthesia will be induced with 1-8% sevoflurane via a facemask. Anaesthesia will be maintained with 1 minimum alveolar concentration (MAC) sevoflurane. Intraoperative monitoring will include pulse oximetry, non-invasive blood pressure, electrocardiogram (ECG), end tidal carbon dioxide concentration and heart rate. An intraoperative increase in respiratory rate, heart rate or mean arterial pressure of >20% following skin incision or during surgery will be defined as insufficient analgesia and treated with 0.25 ug/kg fentanyl intravenously. Local wound infiltration Once general anaesthesia has been established the surgeon will perform all subcutaneous periumbilical local anaesthetic infiltrations. Following aseptic preparation of the site a total of 0.3ml/kg (to a maximum of 5ml) of combined 1% lignocaine and 1% ropivacaine will be infiltrated 5 minutes prior to skin incision. Ultrasound guided Rectus sheath blocks Once general anaesthesia has been established the primary investigator, or consultant anaesthetist experienced in ultrasound-guided regional anaesthesia in children, will perform the bilateral rectus sheath block. A Micromaxx ultrasound machine with either a hockey stick or high frequency linear (HFL) probe will be used to identify the relevant structures within the rectus sheath. Following aseptic preparation of the puncture site and the ultrasound probe, the rectus sheath block will be performed under cross-sectional continuous ultrasound imaging. A 22g spinal needle will be used to facilitate placement on both sides of the umbilicus. The injection site will be defined where the optimal ultrasonic visualisation of the posterior sheath is achieved. Once the needle is correctly positioned within the rectus sheath a predetermined volume of 1% lignocaine and 1% Ropivacaine will be injected following a negative aspiration test. A total of 0.3ml/kg (to a maximum of 5ml) of combined 1% lignocaine and 1% ropivacaine will infiltrated bilaterally 5 minutes prior to skin incision.

Sponsors

Dr Michael Fredrickson
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
1 Weeks to 14 Years
Healthy volunteers
No

Inclusion criteria

Paediatric patients requiring umbilical hernia repair

Exclusion criteria

1. Patient refusal / inability to obtain consent. 2. Allergy amide LA drugs 3. History of seizures or neurological disorders 4. Infection at site of needle puncture 5. Inability to visualise posterior rectus sheath on ultrasound

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026