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Clinical Trials/NCT06391541
NCT06391541
Active, Not Recruiting
N/A

Comparison of the Effects of Modified Thoracolumbar Interfacial Plan Block (mTLIP) and Intertransverse Process Block in Lumbar Disc Surgery

Zonguldak Bulent Ecevit University1 site in 1 country90 target enrollmentApril 1, 2024
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ConditionsLumbar Disc HerniationPain, PostoperativeRegional Aneshesia

Overview

Phase
N/A
Intervention
Not specified
Conditions
Lumbar Disc Herniation
Sponsor
Zonguldak Bulent Ecevit University
Enrollment
90
Locations
1
Primary Endpoint
postoperative opioid consumption
Status
Active, Not Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

to compare ultrasonography (USG)-guided intertransverse process block and modified thoracolumbar interfascial plan (mTLIP) block in the treatment of postoperative pain in patients undergoing lumbar disc herniation surgery under general anesthesia.

Registry
clinicaltrials.gov
Start Date
April 1, 2024
End Date
June 30, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Zonguldak Bulent Ecevit University
Responsible Party
Principal Investigator
Principal Investigator

Çağdaş Baytar

Principal Investigator

Zonguldak Bulent Ecevit University

Eligibility Criteria

Inclusion Criteria

  • •18-75 years old
  • •ASA I-II-III risk group
  • •Patients whose consent was obtained with an informed consent form
  • •Patients who will undergo lumbar disc herniation surgery

Exclusion Criteria

  • •Patients who refused to participate in the study
  • •Allergic to local anesthetics
  • •Patients with coagulopathy
  • •Infection at the site of intervention
  • •Patients under 18 years of age
  • •Patients with ASA score IV and above
  • •Chronic pain disorders
  • •Those with neurological or neuromuscular disease
  • •Patients with psychiatric problems
  • •Patients with a history of opioid use

Outcomes

Primary Outcomes

postoperative opioid consumption

Time Frame: up to 24 hours after surgery

total amount of opioids consumed in 24 hours postoperatively

Secondary Outcomes

  • incidence of nausea and vomiting(up to 24 hours after surgery)
  • Quality of Recovery-15 scale(24 hours after surgery)
  • pain scores(up to 24 hours after surgery)

Study Sites (1)

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