ClinicalTrials.Veeva

Menu

Influence of the Dominance of the Shoulder Stabilized by the Open Latarjet Procedure on the Functional Recovery of the Shoulder at 4.5 Months Postoperatively. (Dom Lat)

R

Ramsay Générale de Santé

Status

Unknown

Conditions

Shoulder Injuries
Latarjet

Treatments

Behavioral: SI-RSI questionnaire
Other: Different exercises with their shoulders

Study type

Observational

Funder types

Other

Identifiers

NCT05150379
Not yet assigned

Details and patient eligibility

About

The aim of this study is to quantify the functional deficits as a function of the dominance of the shoulder stabilized by the open procedure of Latarjet at 4.5 months postoperatively compared to healthy controls.

Enrollment

162 estimated patients

Sex

All

Ages

15 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

  • Patients from two studies : "Reproducibility of functional tests of the shoulder for the return to sport of patients operated on anterior instability of the shoulder "CPP n ° 2018-A03013-52 and "Validation of the S-STARTS composite score to assess the functions of the shoulder and the patient's ability to return to sport after stabilization of the shoulder by the Latarjet procedure (VAL-S-STARTS)" MR3016020520
  • healthy volunteers from two studies : "Reproducibility of functional tests of the shoulder for the return to sport of patients operated on anterior instability of the shoulder "CPP n ° 2018-A03013-52" and "Risk factors for shoulder dislocation in rugby players. Predictive validity of the S-STARTS composite score "MR4612110620

Inclusion criteria:

Patients: o patient between 15 and 45 years old

  • Occurrence of the injury requiring surgery during a sports activity
  • Reduced shoulder instability by the open Latarjet procedure
  • Surgery performed by surgeons from the Santy Orthopedic Center (Lyon)
  • Inclusion by decision of the surgeon during the visit 4 months postoperatively

Healthy volunteers :

  • volunteer between 15 and 45 years old
  • Practice a regular sporting activity

Both groups:

  • Patient having signed an informed consent
  • Subject affiliated or beneficiary of a social security scheme

Exclusion Criteria:

Patient group:

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

Healthy volunteers :

  • Medical history of upper limb pain / injury within the past 12 months
  • Medical history of orthopedic surgery on the upper limbs

Both groups:

  • Protected subject: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision

Trial design

162 participants in 3 patient groups

Dominant side shoulder surgery patients
Treatment:
Behavioral: SI-RSI questionnaire
Other: Different exercises with their shoulders
Patients operated on the shoulder on the non-dominant side
Treatment:
Behavioral: SI-RSI questionnaire
Other: Different exercises with their shoulders
Healthy volunteers
Treatment:
Behavioral: SI-RSI questionnaire
Other: Different exercises with their shoulders

Trial contacts and locations

1

Loading...

Central trial contact

Jean-François Oudet; Marie-Hélène Barba

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems