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Sacral Erector Spinae Plane Blocks in Pediatric Patients

Retrospective Analyses of Sacral Erector Spinae Plane Blocks in Pediatric Patients: Is it Time to Discuss the Necessity of Caudal Block

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05415046
Enrollment
15
Registered
2022-06-10
Start date
2022-06-15
Completion date
2022-07-08
Last updated
2022-08-17

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

Conditions

Postoperative Pain

Brief summary

Patients who were operated by Department of Pediatric Surgery and who received sacral erector spinae plane blocks as a part of postoperative analgesia management will be scanned.

Detailed description

Erector spinae plane block (ESPB) is a safe and effective regional anesthesia technique in pediatric patients and can be performed at any level of the thoracic and lumbar vertebrae. In addition, ESPB can be performed at the sacral region in the midline. In pediatric patients, sacral ESPB provides effective analgesia and this method can replace caudal blocks. This study aims to investigate the efficacy of sacral ESPB retrospectively. Demographical data of the patient, indication/surgery type, total volume applied, additional analgesic use, type of the analgesic if used will be investigated.

Interventions

PROCEDURESacral ESPB

Erector spinae plane block performed with 0,25% bupivacaine (1 mL/kg-max 20mL), under general anesthesia before the start of the surgery.

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years

Inclusion criteria

* Patients who were operated by Department of Pediatric Surgery

Exclusion criteria

* Incomplete patient forms

Design outcomes

Primary

MeasureTime frameDescription
Face, Legs, Activity, Cry, Consolability (FLACC) ScalePostoperative 24th hour.The scale is scored in a range of 0-10 with 0 representing no pain (meaning a better outcome). The scale has five criteria, which are each assigned a score of 0, 1 or 2.
Rescue analgesic-paracetamolDuring the postoperative 24th hour.The need and amount of the IV paracetamol given
Rescue analgesic-ibuprofenDuring the postoperative 24th hour.The need and amount of the oral ibuprofen given

Countries

Turkey (Türkiye)

Outcome results

None listed

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