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mTLIP vs. ITP Blocks in Lumbar Disc Surgery

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

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06391541
Enrollment
90
Registered
2024-04-30
Start date
2024-04-01
Completion date
2025-06-30
Last updated
2024-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Disc Herniation, Pain, Postoperative, Regional Aneshesia

Keywords

postoperative pain, opioid consumption, Pain management, nerve blocks, QoR-15

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.

Interventions

PROCEDUREmodified thoracolumbar interfacial plan block (mTLIP)

Injecting local anesthetic at L3 vertebral level between the longisimus and iliocostalis muscles within the erector spinae muscles.

injection of local anesthetic on the superior costotransverse ligament between the transverse process and the pleura.

Sponsors

Zonguldak Bulent Ecevit University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

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 * Chronic use of NSAIDs * Those contraindicated for regional anesthesia * Patients with a history of opioid use * Chronic analgesic use

Design outcomes

Primary

MeasureTime frameDescription
postoperative opioid consumptionup to 24 hours after surgerytotal amount of opioids consumed in 24 hours postoperatively

Secondary

MeasureTime frameDescription
pain scoresup to 24 hours after surgeryPatients will be evaluated at regular intervals after surgery and their pain will be measured using a numerical rating scale.
incidence of nausea and vomitingup to 24 hours after surgerynausea and vomiting of postoperative patients will be evaluated
Quality of Recovery-15 scale24 hours after surgeryThe quality of recovery of patients will be assessed with the quality of recovery 15 questionnaire.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 16, 2026