ClinicalTrials.Veeva

Menu

Evaluation of Factors Associated With Return to Sports Activity Six Months After Anterior Shoulder Stabilisation With Latarjet. (ERASME)

G

GCS Ramsay Santé pour l'Enseignement et la Recherche

Status

Completed

Conditions

Shoulder Luxation

Treatments

Procedure: Latarjet

Study type

Observational

Funder types

Other

Identifiers

NCT05010278
COS-RGDS-2020-06-024

Details and patient eligibility

About

On a population of sports patients who had undergone a Latarjet operation for post-traumatic anterior shoulder instability, reviewed in consultation 6 months after the operation as part of an ordinary follow-up and divided into two groups according to their current sports practice.

Group 1: "SUCCESS": return to the same level in the same sport. Group 2: "FAILURE": return to the same sport with a reduced level or change of sport or significant reduction or cessation of sporting activity.

Full description

Primary objective:

to assess the impact of patients' psychological state on failure to return to sport.

Secondary objectives:

  • To compare the functional assessment of the shoulder of patients for whom return to sport is successful or unsuccessful (Walch score, isokinetic tests and CKCUES Test score)
  • To describe the factors associated with failure to return to sport

Enrollment

118 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient aged 18 years or older, having been informed of the research
  • Sports patients who have expressed their desire to resume their sporting activity
  • Patient who has undergone a first intention Latarjet operation
  • Patient regularly monitored since the operation and for whom all the data collected during the six-month follow-up visit are available

Exclusion criteria

  • Patient operated for revision surgery
  • Patient with an associated rotator cuff or biceps injury
  • Patient under court protection, guardianship or curatorship
  • Patient who has indicated his opposition to the use of his medical data (by completing and returning the non-opposition form which will be sent to him)

Trial design

118 participants in 1 patient group

Latarjet
Description:
Patients followed up 6 months after a Latarjet procedure
Treatment:
Procedure: Latarjet

Trial contacts and locations

1

Loading...

Central trial contact

Alexandre HARDY, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems