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Glenoid Labrum Tear clinical trials

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NCT ID: NCT05800184 Recruiting - Shoulder Pain Clinical Trials

Finnish Imaging of Shoulder Trauma

FIMAGE-T
Start date: April 5, 2023
Phase:
Study type: Observational

The FIMAGE-Trauma study is an extension of the FIMAGE study and aims to answer the question if rotator cuff tears found on shoulder imaging after a shoulder injury are caused by the index trauma or are rather incidental findings. Eligible participants of the FIMAGE study will be invited to a follow up visit in the case of a shoulder injury or a sudden onset of significant shoulder symptoms (within a 2-year time frame). These findings will then be compared to the baseline data collected in the FIMAGE study (including the comparison of pre-injury and post-injury MRI:s)

NCT ID: NCT05641415 Active, not recruiting - Shoulder Pain Clinical Trials

Finnish Imaging of Shoulder Study

FIMAGE
Start date: January 30, 2023
Phase:
Study type: Observational

In the Finnish Imaging of Shoulder study we will recruit 600 participants from a nationally representative general population sample. Participants aged 40 to 75 years will be invited to a clinical visit that includes assessment of general health, shoulder history and symptoms, and bilateral clinical examination and shoulder imaging (both plain radiography and MRI). We aim to assess the prevalence of abnormal imaging findings in both asymptomatic and symptomatic individuals and explore possible risk factors for abnormal imaging findings and shoulder symptoms.

NCT ID: NCT03675620 Withdrawn - Glenoid Labrum Tear Clinical Trials

Blood Flow Restriction Training Following Glenoid Labral Repair

Start date: January 31, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effects of BFR training on patient reported outcome measures and shoulder muscle girth in patients following glenoid labral repair. The investigators hypothesize that participants receiving BFR with rehabilitation will have greater improvements in patient reported outcome measures and shoulder muscle girth than participants who are treated without BFR.