Case Study: HAGL-lesion (HAGL:Humeral Avulsion Glenohumeral Ligament)

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

6 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-11-30

Study Completion Date

2014-03-31

Brief Summary

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This study shows a new technique which has been implemented at the schulthess clinic to improve the outcome after an correction of an anterior instability in the shoulder joint due to a HAGL lesion.

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Detailed Description

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The aim of the study is to describe and document the results of a case serie after an arthroscopically intervention to correct the anterior instability in the shoulder joint with one primary parameter (WOSI-Score) and several secondary parameters, which are used in the daily clinical routine (e.g.clinical examination, several questionnaires). The results of these parameters will be used to document the mid-term results (\> 1 year after surgery).

Conditions

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Shoulder Injuries and Disorders

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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New Technique

All patients who underwent surgical repair of the anterior instability due an HAGL lesion.

Arthroscopically repair of the anterior shoulder instability

Intervention Type PROCEDURE

Arthroscopically repair of the anterior shoulder instability

Interventions

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Arthroscopically repair of the anterior shoulder instability

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* arthroscopically repair of the anterior instability of the shoulder due an HAGL lesion (performed by Dr. M. Flury, Dr. H.-K. Schwyzer or Dr. Ph. Frey at the Schulthess Klinik)
* patients ≥18 years
* written informed consent

Exclusion Criteria

* additional surgeries at the affected side after the index surgery (arthroscopically repair of the anterior instability due an HAGL lesion)
* non-compliance
* disorders which handicap or inhibit the patient to follow the orders of the clinical testers
* request of the patient

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No