US-Guided Superficial Cervical Plexus Block

NCT ID: NCT03933566

Last Updated: 2024-04-09

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

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-05-01

Study Completion Date

2020-08-01

Brief Summary

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This retrospective observational study compare ultrasound-guided plane and landmark-based superficial cervical plexus block

Detailed Description

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Traditionally, the superficial cervical plexus is blocked using a subcutaneous infiltration of local anesthetics along the posterior border of the sternocleidomastoid muscle.Recently, ultrasound has been used to identify intermuscular planes to carry out transversus abdominis plane and obturator nerve blocks.Thus, to validate this new method, the investigators conducted a retrospective observational study comparing ultrasound and the conventional landmark-based technique for superficial cervical plexus.

Conditions

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Nerve Block

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Ultrasound-Guided

Ultrasound-Guided Superficial Cervical Plexus Block

Ultrasound-Guided Superficial Cervical Plexus Block

Intervention Type PROCEDURE

Ultrasound-Guided Superficial Cervical Plexus Block

Landmark-Based

Landmark-Based Superficial Cervical Plexus Block

Landmark-Based Superficial Cervical Plexus Block

Intervention Type PROCEDURE

Landmark-Based Superficial Cervical Plexus Block

Interventions

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Ultrasound-Guided Superficial Cervical Plexus Block

Ultrasound-Guided Superficial Cervical Plexus Block

Intervention Type PROCEDURE

Landmark-Based Superficial Cervical Plexus Block

Landmark-Based Superficial Cervical Plexus Block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Undergoing surgery of the shoulder and clavicle
* Urgent or planned surgery

Exclusion Criteria

* Refused to sign informed consent
* Pregnant women
* Allergic to the local anesthetic
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ruizhao Lv, M.D

Role: PRINCIPAL_INVESTIGATOR

Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Locations

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Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Cangzhou, Hebei, China

Site Status

Countries

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China

Other Identifiers

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2019CZTCWM2

Identifier Type: -

Identifier Source: org_study_id

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