Follow-up Study After Bankart Repair Using MG-1

Johnson & Johnson (J&J)

Status: Completed

Conditions: Shoulder Dislocation

Study type: Observational

Funder types: Industry

Identifiers

NCT02228226

JJKK-MIT-002

Details and patient eligibility

About

Long term follow-up of patients those who underwent arthroscopic Bankart repair using MG-1 for dislocation of shoulder to evaluate anchor bone hole condition and ossification.

Enrollment: 11 patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient who was enrolled to the clinical trial of MG-1 at Funabashi Orthopaedic Hospital and who don't withdraw the consent
• Patient who understand the contents of the study and from whom a written consent can be obtained

Exclusion criteria

• Patient with dementia
• Patient who cannot undergo CT examination
• Patient who underwent further surgery to ipsilateral shoulder joint after the clinical trial
• Patient who is pregnant or lactating
• Patient judged to be inappropriate for the study by the (sub)investigator

Trial design

11 participants in 1 patient group

MG-1treated group

Description:

MG-1treated group: Patients those who underwent arthroscopic Bankart repair for glenohumeral instability using MG-1