Analgesia for Clavicular Fracture and Surgery

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03933228

Enrollment

150

Registered

2019-05-01

Start date

2019-05-01

Completion date

2022-03-01

Last updated

2024-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clavicular Fractures

Keywords

Combined Interscalene-Cervical Plexus Block, Combined Supraclavicular-Cervical Plexus Block

Brief summary

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

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.

Interventions

PROCEDUREInterscalene-Cervical Plexus Block

Ultrasound-Guided Combined Interscalene-Cervical Plexus Block

PROCEDURESupraclavicular-Cervical Plexus Block

Ultrasound-Guided Combined Supraclavicular-Cervical Plexus Block

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

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

Secondary

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

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026