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

• Sponsor: Schulthess Klinik (Other)
• Overall Status: Completed
• CT.gov ID: NCT01805050
• Collaborator: (none)
• Enrollment: 6
• Location: 1
• Duration (Months): 3.9
• Patients Per Site Per Month: 1.5

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Shoulder Injuries and Disorders	Procedure: Arthroscopically repair of the anterior shoulder instability

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 Design

• Study Type: Observational
• Actual Enrollment: 6 participants
• Observational Model: Cohort
• Time Perspective: Other
• Official Title: Arthroscopically Repair of the Anterior Instability of the Shoulder Due an HAGL - Lesion - A Case Serie
• Study Start Date: Nov 1, 2013
• Actual Primary Completion Date: Mar 1, 2014
• Actual Study Completion Date: Mar 1, 2014

Arms and Interventions

Arm	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

Outcome Measures

Primary Outcome Measures

1. WOSI-Score [expected average of 2 years]

Secondary Outcome Measures

1. Sociodemographic Dates [expected average of 2 years]

2. x-ray images [expected average of 2 years]

3. Constant-Murley Score [expected average of 2 years]

4. Rowe - Score [expected average of 2 years]

5. SSV (Simple Shoulder Value) [expected average of 2 years]

6. SST (Simple Shoulder Test) [expected average of 2 years]

7. Measurement of the abduction strength [expected average of 2 years]

8. Measurement of the external rotation strength [expected average of 2 years]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Schulthess Klinik	Zürich	Canton of Zürich	Switzerland

Sponsors and Collaborators

• Schulthess Klinik

Investigators

• Principal Investigator: Matthias Flury, Dr, Upper Extremities Department

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Matthias Flury, Principal Investigator (Department of Upper Extremity), Schulthess Klinik
• ClinicalTrials.gov Identifier: NCT01805050
• Other Study ID Numbers: HAGL
• First Posted: Mar 5, 2013
• Last Update Posted: Mar 22, 2017
• Last Verified: Mar 1, 2017

• Keywords provided by Matthias Flury, Principal Investigator (Department of Upper Extremity), Schulthess Klinik: HAGL; Shoulder instability
• Additional relevant MeSH terms: Shoulder Injuries

Study Results

No Results Posted as of Mar 22, 2017