Analgesia for Clavicular Fracture and Surgery

April 8, 2024 updated by: Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Ultrasound-Guided Combined Interscalene-Cervical Plexus Versus Combined Supraclavicular-Cervical Plexus Block for Surgical Anesthesia in Clavicular Fractures: A Retrospective Observational Study

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

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.

Study Type

Observational

Enrollment (Actual)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • China
    • Hebei
      • Cangzhou, Hebei, China, 061001
        • Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

150

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Interscalene-Cervical Plexus Block
Ultrasound-Guided Combined Interscalene-Cervical Plexus Block
Procedure: Interscalene-Cervical Plexus Block
Ultrasound-Guided Combined Interscalene-Cervical Plexus Block
Supraclavicular-Cervical Plexus Block
Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block
Procedure: Supraclavicular-Cervical Plexus Block
Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Block success rate
Time Frame: At time 15 minutes after the block
Sensory blockade was assessed using the pinprick test at the surgery site
At time 15 minutes after the block

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acute complications
Time Frame: At the end of surgery immediately
Number of participants with phrenic nerve palsy
At the end of surgery immediately

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Investigators

  • Principal Investigator: Ruizhao Lv, M.D, Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2019

Primary Completion (Actual)

December 1, 2021

Study Completion (Actual)

March 1, 2022

Study Registration Dates

First Submitted

April 28, 2019

First Submitted That Met QC Criteria

April 28, 2019

First Posted (Actual)

May 1, 2019

Study Record Updates

Last Update Posted (Actual)

April 9, 2024

Last Update Submitted That Met QC Criteria

April 8, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2019CZTCWM4

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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