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Brachial Plexus Block in Children and Adolescents

Brachial Plexus Block in Children and Adolescents Requiring Surgery Following Trauma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03842423
Enrollment
2760
Registered
2019-02-15
Start date
2002-01-01
Completion date
2018-10-31
Last updated
2019-02-15

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

Conditions

Upper Extremity Fracture

Brief summary

This study involves a retrospective evaluation of brachial plexus anaesthesia in children and adolescents (patients under the age of 18) undergoing surgical procedures of the upper extremity following trauma. The investigators plan to recruit patients from our hospital patient database meeting our inclusion criteria. Observational period was defined between 1st of January 2002 and 31st of October 2018. Necessity to convert to general anaesthesia was defined as primary endpoint.

Interventions

PROCEDUREBrachial Plexus Anaesthesia

Regional anaesthesia for treatment of upper extremity injuries.

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* Brachial plexus anaesthesia for surgical intervention of upper extremity injuries

Exclusion criteria

* age above 18

Design outcomes

Primary

MeasureTime frameDescription
Conversion to general anaesthesiaintraoperativelyThe necessity to convert to general anaesthesia will be obtained from surgery and anaesthesiology protocols and serves as primary outcome to evaluate efficacy of the investigated method of anaesthesia. All patients who received plexus brachialis anaesthesia but had to be converted to general anaesthesia during or prior the surgical intervention will assigned to this outcome measurement. Number of patients who required conversion will be given as percentage of total patient collective. Possible variables: e.g. 0=no conversion, 1=conversion.

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026