Randomized Controlled Comparison of Pre-op TLIP Vs Intra-op TLIP

Description

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.

Conditions

Pain, Spine Fusion

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Study Overview

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Study Details

Study overview

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.

Randomized Controlled Comparison of Preoperative Ultrasound Guided TLIP Block Versus Intraoperative Non-ultrasound Guided TLIP Block

Randomized Controlled Comparison of Pre-op TLIP Vs Intra-op TLIP

Condition
Pain
Intervention / Treatment

-

Contacts and Locations

Royal Oak

William Beaumont Hospital, Royal Oak, Michigan, United States, 48073

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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
  • * younger than 18 years of age on the date of service
  • * does not consent to participating in the program or to be refusal to follow-up at 2-3 weeks, 4-6 weeks, and 3 months post-operatively
  • * requiring revision surgery at the same level for posterior laminectomy with fusion
  • * a daily MME score \>25 MME/day in the pre-operative period will be excluded
  • * a positive drug screen for cocaine and/or tetrahydrocannabinol (THC), defined in the standard Corewell Drugs of Abuse Screening as cocaine \> 300 ng/mL and cannabinoid \> 50 ng/mL-any
  • * ongoing lawsuits, workers compensation, and litigation will be excluded.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

William Beaumont Hospitals,

Daniel Park, MD, PRINCIPAL_INVESTIGATOR, William Beaumont Hospitals

Study Record Dates

2025-10