TLIP Block Versus Modified TLIP Block for Posterior Decompression and Stabilization Surgery

Perioperative Analgesia Efectivity of Thoracolumbar Interfascial Plane Block Compared Modified Thoracolumbar Interfascial Plane Block in Posterior Lumbal Decompression and Stabilization: Research in Intraoperative Hemodynamic and qNox and Total Morfin Comsumption and Postoperative IL-6 Concentration

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05104203

Enrollment

Registered

2021-11-02

Start date

2021-01-21

Completion date

2021-09-28

Last updated

2021-11-02

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

Conditions

Analgesia, Surgical Procedure, Unspecified

Keywords

Erector Spinae Plane Block, opioid consumption, numerical rating scale, Interleukin 10, Interleukin 6, Thoracolumbal Interfascial Plane Block

Brief summary

This study aimed to compare the analgesia effectivity of TLIP and modified TLIP block in Posterior Lumbar Decompression and Stabilization Surgery Perioperatively.

Detailed description

This study aimed to compare the analgesia effectivity of TLIP and modified TLIP block in Posterior Lumbar Decompression and Stabilization Surgery. Intraoperatively, total fentanyl consumption, hemodynamic, and mean qNox Score was recorded. And Postoperatively, the patient was given the PCA, and total morphine consumption was assessed.

Interventions

PROCEDUREThoracolumbar Interfascial Plane block

Interfascial block done by injection between m. multifidus and m. longissimus

PROCEDUREModified Thorcolumbar Interfascial Plane block

Injection of local anesthetics between m. longissimus and m. illiocostalis

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

1. Patients undergo thoracolumbar Decompression and Stabilization Surgery 2. Age between 18-65 years old 3. BMI \>18,5 kg.m2, and BMI\< 30 kg/m2 4. ASA 1-3 5. No contraindications for the patients to do the Block, and the patients agree and signed the informed consent before the procedure was done

Exclusion criteria

1. Obese patient, with BMI\>30 kg.m2 2. Alergic to local anesthetics 3. Underweight patient with BMI \<18,5 kg/m2

Design outcomes

Primary

Measure	Time frame	Description
Hemodynamic	approximately 15 minutes within surgery	Stability of Hemodynamics that needs the fentanyl addition

Secondary

Measure	Time frame	Description
qNox Score	before induction of anesthesia, 15, 30, 45 minutes after the block was done.	qNox score were taken before induction of anesthesia, 15, 30 and 45 minutes after the block done. the mean of 15,30 and 45 minutes qNox score was assesed

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026