Status:
COMPLETED
IV Lidocaine Analgesia in Pediatric Scoliosis Surgery
Lead Sponsor:
University of British Columbia
Conditions:
Scoliosis; Adolescence
Anesthesia Recovery Period
Eligibility:
All Genders
10-19 years
Phase:
PHASE3
Brief Summary
Surgical correction of scoliosis in children is a long procedure, with an equivalently long recovery time, that is commonly performed at BC Children's Hospital. Treating pain immediately after the pro...
Detailed Description
Objectives: The primary objective of this study is to determine if perioperative IV lidocaine therapy (P-IVLT) reduces 48-hour post-operative morphine utilization compared with a control, in adolesce...
Eligibility Criteria
Inclusion
- ASA I-III
- Diagnosed with Idiopathic scoliosis
- Undergoing single-stage posterior spinal instrumentation and fusion
Exclusion
- Thorascopic tethering procedure
- Two-stage procedure
- Abnormal developmental profile
- Congenital/neuromuscular scoliosis
- Requiring PICU admission
- Known allergy to lidocaine
- Known cardiac, renal or liver disease or dysfunction
- Pre-existing pain complaints, i.e. on regular analgesic medications
- Current psychiatric diagnosis, e.g. anxiety, depression, eating disorder, defined according to DSM criteria.
- Requiring non-standard post-op pain management
- Any history of seizures
- Unplanned staged procedure
- Weight \< 5th centile or \> 85th centile for age
- Porphyria
Key Trial Info
Start Date :
December 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 10 2024
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT04069169
Start Date
December 18 2019
End Date
May 10 2024
Last Update
May 14 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
BC Children's Hospital - Department of Anesthesia
Vancouver, British Columbia, Canada, V6H 3V4