Randomized Controlled Comparison of Preoperative Ultrasound Guided TLIP Block Versus Intraoperative Non-ultrasound Guided TLIP Block
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
Single-center, randomized study will enroll 50 subjects who are scheduled for 1-3 level posterior laminectomy \& fusion. Study participants who are eligible for the posterior lumbar laminectomy and fusion procedure will be scheduled and also consented as a part of the study. Participants will be stratified based on age and gender to ensure equal distribution.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• greater than or equal to 18 years of age on the date of service
• require a 1 to 3 level posterior laminectomy with fusion
• compliant with study requirements and outpatient follow-up
• a daily MME less than 25 MME per day in the per-operative period
Locations
United States
Michigan
William Beaumont Hospital
RECRUITING
Royal Oak
Contact Information
Primary
Grace SanAgustin, RN
grace.sanagustin@corewellhealth.org
248-551-6679
Time Frame
Start Date: 2024-10-28
Estimated Completion Date: 2025-10
Participants
Target number of participants: 50
Treatments
Active_comparator: Preoperative Ultrasound TLIP Group
Participant will receive TLIP in preop with 20cc of 0.2% ropivacaine administered bilaterally, 40cc total. Blocks will be performed under ultrasound guidance with an in-plane technique by a single study investigator.
Active_comparator: Intraoperative TLIP Group
Participants will receive TLIP with 20cc of 0.2% ropivacaine bilaterally, 40cc total. Blocks will be performed intraoperatively under direct surgical visualization.
Related Therapeutic Areas
Sponsors
Leads: William Beaumont Hospitals