Status:
TERMINATED
Single vs Double Epidural Catheter Analgesia for Scoliosis Surgery
Lead Sponsor:
University of Wisconsin, Madison
Conditions:
Adolescent Idiopathic Scoliosis
Eligibility:
All Genders
11-18 years
Phase:
NA
Brief Summary
This is a study comparing pain control utlilizing one or two epidural catheters, along with a hydromorphone PCA, for analgesia following surgery for correction of scoliosis.
Eligibility Criteria
Inclusion
- Patients undergoing surgery via a posterior approach for AIS
- Children ages 11-18
- ASA physical status 1-2
- Informed consent by legal guardian and assent by patient (for minors 11-17 years of age) or informed consent by subject (for patients 18 years of age)
- Planned correction of at least 8 vertebral levels
Exclusion
- Patient refusal to participate
- Patients on chronic narcotic medication
- Allergy to standard of care drugs used in the study (Omnipaque, ropivacaine, hydromorphone, oxycodone, acetaminophen, gabapentin, ondansetron, nalbuphine or diphenhydramine, diazepam)
- Coagulopathy
- Pre-existing neurological deficit
- Inability to use a Numerical Rating Scale (NRS: 0-10 patient self-reported score) for pain assessment
Key Trial Info
Start Date :
July 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2014
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT01900626
Start Date
July 1 2013
End Date
December 1 2014
Last Update
May 8 2019
Active Locations (1)
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1
American Family Children's Hospital
Madison, Wisconsin, United States, 53792