CClinicalTrials.gg
WithdrawnNCT06154980Updated Oct 23, 2025

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

An interventional study of Preoperative Ultrasound TLIP and Intraoperative TLIP in Pain and Spine Fusion, sponsored by Corewell Health East. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-10-23.

Sponsored by Corewell Health East · Not applicable, Interventional, and Treatment

Why this study was withdrawn
Physician is leaving the institution and it will not be continued.
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

This is a single-center, randomized study. The study will enroll 50 subjects who are scheduled for 1-3 level posterior laminectomy \& fusion. Potential participants who are eligible for the posterior lumbar laminectomy and fusion procedure will be scheduled as a study participant, consented as a part of the study, and stratified based on age and gender to ensure equal distribution.

For each participant, demographics including age, sex, smoking and alcohol use history, body mass index (BMI), Cranial Cervical Instability (CCI), American Society of Anesthesiology classification (ASA), prior opioid use for pain management, pain levels, function, and prior history of other spinal surgery will be collected prior to surgery. Participants will be randomly assigned to one of two treatment groups: Pre-op ultrasound Thoracolumbar Interfacial Plane Block (TLIP) group or Intra-operative Thoracolumbar Interfacial Plane Block (TLIP) group.

The participant will then undergo the planned 1 to 3 level posterior lumbar laminectomy and fusion procedure.

Post-operative opioid analgesia will be assessed using the Visual Analog Scale (VAS) upon arrival to the post-anesthesia unit (PACU) until discharge and in the outpatient setting. Pain, satisfaction, and opioid analgesia consumption will also be assessed at 2-3 weeks post-operatively, 4-6 weeks post-operatively, and 3 months post-operatively. Pain will be assessed using VAS. Satisfaction will be assessed using a Likert scale. Opioid analgesia is defined as oxycodone, oxymorphone, hydrocodone, hydromorphone, fentanyl, morphine, codeine, methadone, tramadol, and buprenorphine. Opioid consumption will be measured in morphine milligram equivalents (MME).

02

Conditions studied

  • Pain
  • Spine Fusion

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Keywords

  • thoracolumbar interfacial plane block
  • lumbar spine fusion
  • posterior laminectomy with fusion
03

In context

Pain

2,219 studies on the registry are indexed under Pain; 917 are open to participants now.

Browse Pain studies →

Lead sponsor

Corewell Health East is the lead sponsor of 17 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion 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

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • 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.

    Procedure: Preoperative Ultrasound TLIP

  • 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.

    Procedure: Intraoperative TLIP

Interventions

  • ProcedurePreoperative Ultrasound TLIP

    TLIP will be performed in preop with 20cc of 0.2% ropivacaine administered bilaterally, 40cc total. Blocks will be performed under ultrasound guidance with an in-plane technique.

  • ProcedureIntraoperative TLIP

    TLIP will be performed intraoperatively with 20cc of 0.2% ropivacaine bilaterally, 40cc total. Blocks under direct surgical visualization.

06

What researchers measure

Primary outcomes

  1. Pain scores at admission to PACU

    Post operative pain scores will be measured using visual analog scale (VAS) scores at admission to PACU after surgery. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: Baseline (up to 30 days prior to surgery) to PACU admission (immediately post-operative)

  2. Pain scores at admission to inpatient unit

    Post operative pain scores will be measured using visual analog scale (VAS) scores at admission to inpatient unit after surgery. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: At inpatient unit admission (within 24 hours after surgery)

  3. Pain score at discharge from hospital

    Post operative pain scores will be measured using visual analog scale (VAS) scores at every 8 hours after admission to an inpatient unit until discharge. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: At hospital discharge (within 3 days of hospital discharge)

  4. Pain score at 2-3 weeks (VAS)

    Post operative pain scores will be measured using visual analog scale (VAS) scores at the 2-3 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 2-3 weeks after surgery

  5. Pain score at 4-6 weeks (VAS)

    Post operative pain scores will be measured using visual analog scale (VAS) scores at the 4-6 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 4-6 weeks after surgery

  6. Pain score at 3 months (VAS)

    Post operative pain scores will be measured using visual analog scale (VAS) scores at the 3 month follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 3 months after surgery

  7. Pain score at 2-3 weeks (Likert)

    Post-operative pain will be measured using a 10 point Likert pain score. The scale is 1 - 10 and a lower number indicates less pain. 1 is no pain and 10 is intense pain.

    Time frame: 2-3 weeks after surgery

  8. Pain score at 4-6 weeks (Likert)

    Post-operative pain will be measured using a 10 point Likert pain score. The scale is 1 - 10 and a lower number indicates less pain. 1 is no pain and 10 is intense pain.

    Time frame: 4-6 weeks after surgery

  9. Pain score at 3 months (Likert)

    Post-operative pain will be measured using a 10 point Likert pain score. The scale is 1 - 10 and a lower number indicates less pain. 1 is no pain and 10 is intense pain.

    Time frame: 3 months after surgery

  10. Change in pain 24 hours after surgery

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 24 hours after surgery. Pain scores will be measured using visual analog scale (VAS) scores. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 24 hours after surgery

  11. Change in back pain at 2-3 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 2-3 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 2-3 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 2-3 weeks after surgery

  12. Change in back pain at 4-6 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 4-6 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 4-6 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 4-6 weeks after surgery

  13. Change in back pain at 3 months

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 3 months after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 3 month follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 3 months after surgery

  14. Change in right leg pain at 2-3 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 2-3 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 2-3 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 2-3 weeks after surgery

  15. Change in right leg pain at 4-6 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 4-6 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 4-6 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 4-6 weeks after surgery

  16. Change in right leg pain at 3 months

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 3 months after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 3 month follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 3 months after surgery

  17. Change in left leg pain at 2-3 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 2-3 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 2-3 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 2-3 weeks after surgery

  18. Change in left leg pain at 4-6 weeks

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 4-6 weeks after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 4-6 week follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 4-6 weeks after surgery

  19. Change in left leg pain at 3 months

    The change of VAS score from the score at the time of post anesthesia care unit (PACU) arrival to 3 months after surgery. Pain scores will be measured using visual analog scale (VAS) scores at the 3 month follow-up. The scale is 0-10 with a lower score indicating less pain. A score of 0 indicates no pain and a score of 10 indicates severe pain.

    Time frame: 3 months after surgery

  20. Opioid Consumption

    Opioid consumption will be measured in morphine milligram equivalents (MME). This is defined as the amount of milligrams of morphine an opioid dose is equal to. Opioid consumption measured in MME will be collected from PACU through 3 month follow up.

    Time frame: PACU arrival through 3 months

Secondary outcomes

  1. Satisfaction at 3 months

    Satisfaction of surgical outcome will be measured using a 10 point Likert scale. The scale is 1 - 10 and a higher number indicates higher satisfaction with the surgical outcome. 1 is very unsatisfied and 10 is very satisfied.

    Time frame: 3 months after surgery

  2. Satisfaction at 4-6 weeks

    Satisfaction of surgical outcome will be measured using a 10 point Likert scale. The scale is 1 - 10 and a higher number indicates higher satisfaction with the surgical outcome. 1 is very unsatisfied and 10 is very satisfied.

    Time frame: 4-6 weeks after surgery

  3. Satisfaction at 2-3 weeks

    Satisfaction of surgical outcome will be measured using a 10 point Likert scale. The scale is 1 - 10 and a higher number indicates higher satisfaction with the surgical outcome. 1 is very unsatisfied and 10 is very satisfied.

    Time frame: 2-3 weeks after surgery

  4. Number of Adverse Events

    Adverse events will be collected from the time of surgery through 3 months.

    Time frame: Surgery to 3 months

07

Study locations

1 site
  • William Beaumont Hospital
    Royal Oak, Michigan 48073, United States
08

References and documents

Individual participant data

Plan to share: No — Study withdrawn, no individual participant data to share.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 23, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06154980
Lead sponsor
Corewell Health East
Responsible party
Daniel K Park (MD, Orthopedic Surgeon, Corewell Health East) — Principal investigator
First posted
Dec 4, 2023
Start date
Oct 28, 2024
Primary completion
Oct 21, 2025
Completion
Oct 21, 2025
Last update
Oct 23, 2025

Study contacts

Daniel Park, MD
principal investigator · Corewell Health East

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is withdrawn, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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