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NCT02643537 Clinical Trial

Associated Pathologies Following Luxatio Erecta Humeri: A Retrospective Analysis of 31 Cases and Diagnostic Algorithm

Shoulder Dislocation Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02643537
Other study ID # 2009
Secondary ID
Status Completed
Phase N/A
First received December 19, 2015
Last updated December 28, 2015
Start date January 1992

Study information
Verified date December 2015
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Observational

Clinical Trial Summary

The aim of this study was to evaluate the clinical outcome of this rare injury with special emphasis on associated pathologies. Additionally, we aimed to develop an algorithm for the diagnosis of associated pathologies following LEH.

Recruitment information / eligibility
Status Completed
Enrollment 31
Est. completion date
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Included for analysis were all patients over 18 years of age who have been treated for LEH between at our department.

Exclusion Criteria:

- Only injuries of the affected shoulder were taken into account, non-shoulder related pathologies were not addressed.

- Other types of shoulder dislocation except Luxatio erecta

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Medical University of Vienna

Outcome
Type Measure Description Time frame Safety issue
Primary Functional clinical outcome Functional outcome (Range of Motion of the shoulder) at least 2months No
Secondary ASSOCIATED PATHOLOGIES Number of participants with associated pathologies (for example fractures of the greater tuberosity, injuries of the rotator cuff or nerve palsy, e.g.) that were connected with this rare injury at least 2 months No
Secondary Pain Assessment for pain after operative/conservative therapy with the Visual Analog Score for pain at least 2 months No
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