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Regional Anesthesia in Pediatric Orthopaedic Patients

Single-Shot Versus Continuous Regional Anesthesia for Treating Acute Postoperative Pain in Pediatric Orthopaedic Surgery: A Prospective Randomized Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04669145
Enrollment
24
Registered
2020-12-16
Start date
2021-06-24
Completion date
2024-04-22
Last updated
2025-07-29

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

Conditions

Anesthesia, Anesthesia, Local, Orthopedic Disorder

Brief summary

To identify the benefits from regional anesthesia use as pain management in the pediatric population by delineating the differences in efficacy of continuous nerve blockade versus single-shot techniques after pediatric orthopaedic limb procedures. By doing this, the investigators can determine if specific anesthetic techniques should become a standard of care in pain management for the pediatric population and supersede the need for opioid medication.

Interventions

DRUGRopivacaine

Dosing and volume will vary based on type of block used and weight of patient because of the pediatric population in the study.

Sponsors

Ochsner Health System
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing primary orthopaedic limb surgery * Outpatient orthopaedic surgeries * Patients undergoing orthopaedic surgery who would normally receive regional anesthesia

Exclusion criteria

* Patients younger than 5 years of ago or older than 18 years of age * Revision orthopaedic surgeries * Spinal orthopaedic surgeries * Orthopaedic surgeries where the standard of care for type of regional anesthesia has been established (continuous regional for ACL reconstruction) * Patients with the inability to articulate pain scores * Inpatient orthopaedic surgeries * Patients undergoing orthopaedic limb surgery with risk of compartment syndrome (i.e. acute supracondylar humerus fractures)

Design outcomes

Primary

MeasureTime frameDescription
Opioid ConsumptionFor first 48 hours post-operatively.Amount of opioid medications taken for pain control.

Secondary

MeasureTime frameDescription
Opioid ConsumptionThrough 12 hours post-operatively.Amount of opioid medications taken for pain control.
Emergency Room VisitsWithin 2 weeks post-operatively.Emergency room visits due to poor pain control.
Pain ScoresAt 12 hours post-operatively.Universal Pain Assessment tool will be used. The pain scale ranges from 0 to 10 with 0 being no pain and 10 being the worst possible pain.

Countries

United States

Outcome results

None listed

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