mTLIP vs. ITP Blocks in Lumbar Disc Surgery

Not Applicable

Active, not recruiting

• Conditions: Lumbar Disc Herniation; Pain, Postoperative; Regional Aneshesia
• Interventions: Procedure: modified thoracolumbar interfacial plan block (mTLIP); Procedure: Intertransverse process block (ITP)

• Registration Number: NCT06391541
• Lead Sponsor: Zonguldak Bulent Ecevit University

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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-04
• Study Start: 2024-04-01
• Study First Submitted: 2024-04-26
• Study First Submitted QC: 2024-04-29
• Last Update Submitted: 2024-04-29
• Study First Posted: 2024-04-30
• Last Update Posted: 2024-04-30
• Primary Completion: 2025-04-30
• Study Completion: 2025-06-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 90

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group mTLIP	modified thoracolumbar interfacial plan block (mTLIP)	-
Group ITP	Intertransverse process block (ITP)	-

Primary Outcome Measures

Name	Time	Method
postoperative opioid consumption	up to 24 hours after surgery	total amount of opioids consumed in 24 hours postoperatively

Secondary Outcome Measures

Name	Time	Method
incidence of nausea and vomiting	up to 24 hours after surgery	nausea and vomiting of postoperative patients will be evaluated
Quality of Recovery-15 scale	24 hours after surgery	The quality of recovery of patients will be assessed with the quality of recovery 15 questionnaire.
pain scores	up to 24 hours after surgery	Patients will be evaluated at regular intervals after surgery and their pain will be measured using a numerical rating scale.

Trial Locations

Locations (1)

Zonguldak Bülent Ecevit University medicine faculty; 🇹🇷 Zonguldak, Kozlu, Turkey