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

March 20, 2017 updated by: Matthias Flury, Schulthess Klinik

Arthroscopically Repair of the Anterior Instability of the Shoulder Due an HAGL - Lesion - A Case Serie

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

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).

Study Type

Observational

Enrollment (Actual)

6

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

  • Switzerland
    • Canton of Zürich
      • Zürich, Canton of Zürich, Switzerland
        • Schulthess Klinik

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All patients who underwent surgical repair of the anterior instability due an HAGL lesion at the Schulthess Klinik and have been performed surgery by Dr. M. Flury, Dr. H.-K. Schwyzer or Dr. Ph. Frey

Description

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

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

  • Observational Models: Cohort
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
New Technique
All patients who underwent surgical repair of the anterior instability due an HAGL lesion.
Procedure: Arthroscopically repair of the anterior shoulder instability
Arthroscopically repair of the anterior shoulder instability

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
WOSI-Score
Time Frame: expected average of 2 years
expected average of 2 years

Secondary Outcome Measures

Outcome Measure
Time Frame
Sociodemographic Dates
Time Frame: expected average of 2 years
expected average of 2 years
x-ray images
Time Frame: expected average of 2 years
expected average of 2 years
Constant-Murley Score
Time Frame: expected average of 2 years
expected average of 2 years
Rowe - Score
Time Frame: expected average of 2 years
expected average of 2 years
SSV (Simple Shoulder Value)
Time Frame: expected average of 2 years
expected average of 2 years
SST (Simple Shoulder Test)
Time Frame: expected average of 2 years
expected average of 2 years
Measurement of the abduction strength
Time Frame: expected average of 2 years
expected average of 2 years
Measurement of the external rotation strength
Time Frame: expected average of 2 years
expected average of 2 years

Collaborators and Investigators

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

Sponsor

Schulthess Klinik

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

November 1, 2013

Primary Completion (Actual)

March 1, 2014

Study Completion (Actual)

March 1, 2014

Study Registration Dates

First Submitted

March 4, 2013

First Submitted That Met QC Criteria

March 4, 2013

First Posted (Estimate)

March 5, 2013

Study Record Updates

Last Update Posted (Actual)

March 22, 2017

Last Update Submitted That Met QC Criteria

March 20, 2017

Last Verified

March 1, 2017

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HAGL

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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