mTLIP vs. ITP Blocks in Lumbar Disc Surgery

NCT ID: NCT06391541

Last Updated: 2024-04-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2025-06-30

Brief Summary

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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

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Conditions

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Lumbar Disc Herniation Pain, Postoperative Regional Aneshesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Group Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Group mTLIP

Group Type ACTIVE_COMPARATOR

modified thoracolumbar interfacial plan block (mTLIP)

Intervention Type PROCEDURE

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

Group ITP

Group Type ACTIVE_COMPARATOR

Intertransverse process block (ITP)

Intervention Type PROCEDURE

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

Interventions

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modified thoracolumbar interfacial plan block (mTLIP)

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

Intervention Type PROCEDURE

Intertransverse process block (ITP)

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

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Zonguldak Bulent Ecevit University

OTHER

Sponsor Role lead

Responsible Party

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Çağdaş Baytar

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Zonguldak Bülent Ecevit University medicine faculty

Zonguldak, Kozlu, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2024/06-18

Identifier Type: -

Identifier Source: org_study_id

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