Status:

UNKNOWN

Ambulatory Rehabilitation Program in Patients With Degenerative Rupture of the Rotator Cuff Tendons of the Shoulder

Lead Sponsor:

Assistance Publique - Hôpitaux de Paris

Conditions:

Shoulder Pain

Eligibility:

All Genders

55+ years

Phase:

NA

Brief Summary

The main objective of the research is to study the effectiveness of an ambulatory rehabilitation program based on mobilization and muscular solicitation, during painful shoulders by full-thickness deg...

Detailed Description

Our hypothesis is that rehabilitation based on mobilization and muscular solicitation is effective in painful shoulder due to degenerative rupture of the tendons of the rotator cuff; that it reduces p...

Eligibility Criteria

Inclusion

  • Age ≥ 55 years old,
  • Painful shoulder for at least 1 month,
  • Shoulder treated with at least one cortisone infiltration one month or more before inclusion,
  • Pain ≥ 40/100 on visual analog scale,
  • Pain reproduced by at least one clinical test of rotator cuff tendons or subacromial impingement (Jobe, Patte, Neer, Yocum test, Hawkins),
  • Full-thickness tear of at least one tendon of the rotator cuff attested by imaging,
  • Affiliation to social security

Exclusion

  • Passive glenohumeral mobility of the shoulder limited,
  • Calcifying tendinopathy on standard radiography,
  • Glenohumeral arthropathy;
  • Painful acromioclavicular arthropathy;
  • History of shoulder fracture;
  • Neurogenic pain or neurogenic motor deficit of the upper limb;
  • Cortisone infiltration of the shoulder in the month preceding inclusion;
  • Operated shoulder;
  • Systemic pathologies including inflammatory rheumatism or neoplastic pathology;
  • Patient participating in another experimental research;
  • Patient under legal protection (curators or guardianship)
  • Patient deprived of liberty by a judicial or administrative decision
  • Pregnant or breastfeeding woman

Key Trial Info

Start Date :

September 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2024

Estimated Enrollment :

134 Patients enrolled

Trial Details

Trial ID

NCT05413213

Start Date

September 1 2022

End Date

September 1 2024

Last Update

June 9 2022

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