Reproducibility of Functional Shoulder Tests for the Return to Sport of Patients Operated on Previous Shoulder Instability

Ramsay Générale de Santé

Status: Unknown

Conditions: Shoulder Injuries; Latarjet

Treatments: Other: Functional tests

Study type: Interventional

Funder types: Other

Identifiers

NCT05084703

2018-A03013-52

Details and patient eligibility

About

The aim of this study is to assess whether the indicators outcome of these tests discriminate between different populations. In particular to compare populations with shoulders without any history of injury with a population that had undergone a reduction in glenohumeral instability by the Latarjet technique.

Full description

The different objectives of this study are :

• To assess the intra- and intersessional reproducibility of functional shoulder tests
• To evaluate the influence of an anterior front stop using the Latarjet method on the functional profile of the shoulder compared to a healthy population.

Enrollment: 100 estimated patients

Sex: Male

Ages: 18 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Patient group :

• Male patient
• Between 18 and 30 years-old
• Occurrence of the injury requiring surgery during a sports activity
• Reduction of shoulder instability by the Latarjet technique
• Surgery performed by surgeon from Santy orthopedic center (Lyon)
• Patient's inclusion by decision of the surgeon during the 4 months postoperatively visit

Healthy volunteer group :

• Male patient
• Between 18 and 30 years-old
• Patient regularly practicing sport activity.

Both groups :

• Patient having signed an informed consent
• Affiliated subject or beneficiary of a social security scheme

Exclusion criteria

Patient group :

• Contra indication from surgeon
• Having another pathology in the upper limbs
• Present a constitutional hyperlaxity
• Have stiffness or recurrence of dislocation of the shoulder post-surgery

Healthy volunteer group :

• Report a history of upper extremity pain / injury within the past 12 months
• Report a history of orthopedic surgery on the upper limbs

All participants :

• Protected subject : adult under guardianship, guardianship or other legal protection, deprived of liberty by judicial or administrative decision
• pregnant woman, breastfeeding, parturient

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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100 participants in 2 patient groups

Patients operated for previous shoulder instability

Experimental group

Description:

Different functionnal test to be done

Treatment:

Other: Functional tests

Healthy volunteer

Active Comparator group

Description:

Different functionnal test to be done

Treatment:

Other: Functional tests