Analgesia for Clavicular Fracture and Surgery

NCT ID: NCT03933228

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

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-05-01

Study Completion Date

2022-03-01

Brief Summary

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Compared efficacy of ultrasound-guided combined interscalene-cervical plexus versus combined supraclavicular-cervical plexus block for surgical anesthesia in clavicular fractures.

Detailed Description

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The primary objective of this study was to compare the effectiveness of ultrasound-guided combined interscalene-cervical plexus versus combined supraclavicular-cervical plexus block for surgical anesthesia in clavicular fractures.The hypothesis of this study was that the supraclavicular-cervical plexus block could provide better anesthesia with less anesthesia related complications.

Conditions

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Clavicular Fractures

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Interscalene-Cervical Plexus Block

Ultrasound-Guided Combined Interscalene-Cervical Plexus Block

Interscalene-Cervical Plexus Block

Intervention Type PROCEDURE

Ultrasound-Guided Combined Interscalene-Cervical Plexus Block

Supraclavicular-Cervical Plexus Block

Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Supraclavicular-Cervical Plexus Block

Intervention Type PROCEDURE

Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Interventions

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Interscalene-Cervical Plexus Block

Ultrasound-Guided Combined Interscalene-Cervical Plexus Block

Intervention Type PROCEDURE

Supraclavicular-Cervical Plexus Block

Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Surgery of the clavicular fractures under combined cervical plexus plus brachial plexus block
* 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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2019CZTCWM4

Identifier Type: -

Identifier Source: org_study_id

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