Ultrasound-Guided Intermediate Versus Deep Cervical Plexus Block for Carotid Endarterectomy

NCT ID: NCT05353218

Last Updated: 2023-04-28

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

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-06-07

Study Completion Date

2023-04-27

Brief Summary

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Cervical plexus blocks are regional methods used in carotid endarterectomy. Cervical plexus blocks consist of three blocks: superficial, intermediate and deep. These three blocks can be used alone or combined. The aim of this study is to evaluate the effectiveness of ultrasound-guided intermediate and deed cervical plexus block in patients undergoing carotid endarterectomy.

Detailed Description

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Carotid endarterectomy is a surgical method used to treat occlusive lesions of the carotid. Regional anesthesia is preferred because it allows for consciousness control and neurological examination during the operation. Cervical plexus blocks are regional methods used in carotid endarterectomy. It is a regional technique in which the cervical spinal nerves (C2-C3-C4) are blocked with a local anesthetic agent from different regions. Cervical plexus blocks consist of three blocks: superficial, intermediate and deep, depending on the depth at which the local anesthetic agent is infiltrated. According to the preference of the clinician for the purpose of anesthesia, these three blocks can be used separately or combined. It is mentioned that all three blocks provide sufficient anesthesia for carotid endarterectomy surgery to be performed.

In the study, investigators planned to evaluate the effectiveness of ultrasound-guided intermediate and deep cervical plexus blocks in patients undergoing carotid endarterectomy by comparing the number of patients who need additional local anesthetics.

Conditions

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Anesthesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized, Prospective
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Caregivers Investigators Outcome Assessors

Study Groups

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Group intermediate cervical plexus block (GI)

Patients anesthetized with intermediate cervical plexus block.

Group Type ACTIVE_COMPARATOR

Intermediate cervical plexus block

Intervention Type PROCEDURE

Intermediate cervical plexus block will be applied in transverse plane using posterior approach at C4.

Group deep cervical plexus block (GD)

Patients anesthetized with deep cervical plexus block.

Group Type ACTIVE_COMPARATOR

Deep cervical plexus block

Intervention Type PROCEDURE

Deep cervical plexus block will be appliedin transverse plane using anterior approach at C2-3-4.

Interventions

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Intermediate cervical plexus block

Intermediate cervical plexus block will be applied in transverse plane using posterior approach at C4.

Intervention Type PROCEDURE

Deep cervical plexus block

Deep cervical plexus block will be appliedin transverse plane using anterior approach at C2-3-4.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients scheduled for carotid endarterectom y surgery.

Exclusion Criteria

* Local infection
* Previous ipsilateral surgery
* Radiotherapy
* Conversion to general anesthesia
* Known bleeding disorders
* Known allergy of local anesthetic
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University

OTHER

Sponsor Role lead

Responsible Party

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Ozlem Turhan

Specialist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istanbul Faculty of Medicine

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2021/923

Identifier Type: -

Identifier Source: org_study_id

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