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Prospective Descriptive Study of Injuries Associated to Anterior Shoulder Dislocations in Patients Over 40 Years

Prospective Descriptive Study of Injuries Associated to Anterior Shoulder Dislocations in Patients Over 40 Years

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05898243
Enrollment
120
Registered
2023-06-12
Start date
2023-06-01
Completion date
2028-05-31
Last updated
2024-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Glenohumeral Dislocations

Brief summary

The glenohumeral joint has the highest rate of dislocation of the whole body, due to its high mobility and the special characteristics of its anatomy. It is estimated that every year between 1-2% of the population will suffer from glenohumeral dislocation. The vast majority of studies are based on young patients under the age of 40, given that at this age they have the higher incidence and at the same time, they have higher redislocation index. However, the investigators are in front of a more active population with a longer life expectancy. That is why the cases of anterior glenohumeral dislocations are increasing in people older than 40 years. Given that most studies focus on younger patients, the investigators lack knowledge about which injuries are associated with dislocation at this age and whether these influence its clinical evolution.

Interventions

PROCEDUREReduction

An Rx will be performed before and after the reduction of the dislocation. After that, the neurovascular state will be checked and also if there is some associated injury.

Sponsors

Corporacion Parc Tauli
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* More than 40 years old * First episode of traumatic anterior gelnohumeral dislocation seen in Rx * Acceptance to be checked over 2 years * Acceptance to be submitted to TAC, NMR, EMG and Bilateral Ultrasound

Exclusion criteria

* Previous fractures in this extremity * Previous neurovascular lesions in this extremity * Other associated lesions * Cognitive alterations or dementia which prevent completing the protocols. Patients with \<14 points in Mini-mental test.

Design outcomes

Primary

MeasureTime frame
Characterization of associated lesionsAt the three months visit including assessment of NMR/EMG/TAC/Bilateral Ultrasound

Secondary

MeasureTime frame
Constant Functional Test3, 6, 12 and 24 months
WOSI test3, 6, 12 and 24 months
SST3, 6, 12 and 24 months
Redislocations3, 6, 12 and 24 months
Type of treatment3, 6, 12 and 24 months

Countries

Spain

Contacts

Primary ContactMònica Salomó
msalomo@tauli.cat+34 93 723 10 10
Backup ContactMireia Viñas
mmvinas@tauli.cat+34 93 723 10 10

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026