Pain Clinical Trial
Official title:
Prospective Randomized Trial Using Medrol Dose Packs for Post-Operative Pain Control
Verified date | June 2024 |
Source | University of Utah |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators primary purpose of this study is to determine if the addition of a short course use of steroids following surgery for Adolescent Idiopathic Scoliosis (AIS) will improve post-operative pain management and shorten hospital length of stay.
Status | Enrolling by invitation |
Enrollment | 90 |
Est. completion date | January 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 21 Years |
Eligibility | Inclusion Criteria: - age range of 10-21 - received AIS surgery Exclusion Criteria: - participants out of the age range 10-21 - other forms of scoliosis (not AIS) |
Country | Name | City | State |
---|---|---|---|
United States | University of Utah Orthopaedic Center | Salt Lake City | Utah |
Lead Sponsor | Collaborator |
---|---|
University of Utah |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 1, post Adolescent Idiopathic Scoliosis (AIS) surgery | |
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 2, post (AIS) surgery | |
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 3, post (AIS) surgery | |
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 4, post (AIS) surgery | |
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 5, post (AIS) surgery | |
Primary | Visual Analog Scale (VAS) pain | VAS pain score (0 no pain - 10 severe pain) | Day 6, post (AIS) surgery |
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