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Pillow Brace Assessment on Sleep Quality of Patients Undergoing Arthroscopic Rotator Cuff Surgery

RecruitingNAAges 18 Years - anyAllGCS Ramsay Santé pour l'Enseignement et la Recher…
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In plain words

What the trial is, and whether it could suit you

Rotator cuff surgery is an increasingly popular procedure in France. It is a common procedure for patients with shoulder tendon injuries, aimed at restoring mobility and reducing pain. Although arthroscopic techniques have improved functional outcomes, managing postoperative pain, particularly at night, and its consequences remains a major challenge. Studies highlight that postoperative nighttime pain can significantly affect sleep quality, delaying functional recovery and patient satisfaction. However, standard splints used for postoperative immobilization do not offer an optimal solution to this problem, leaving a significant gap in the care of these patients. Given this observation, a splint incorporating a support cushion system could meet the specific needs expressed by patients who have undergone rotator cuff surgery, namely improving sleep quality by minimizing nighttime pain. T

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patient undergoing arthroscopic rotator cuff repair surgery confirmed by clinical diagnosis and preoperative imaging tests. * Patient able to understand the instructions for using the brace. * Patient able to perform activities of daily living with or without a brace, ensuring proper use of the brace. * Patient affiliated with or beneficiary of a social security system * French speaking patient, having signed an informed consent form Exclusion Criteria: * Patient with an uncertain diagnosis * Patient undergoing rotator cuff revision surgery. * Patient with complex or surgical fractures of the shoulder, humerus, or ribs * Patient with multiple fractures, open fractures, or those with pinning * Patient who has undergone multiple surgeries in the last 6 months. * Patient with shoulder pathologies unrelated to the rotator cuff, such as severe arthritis or capsulitis. * Patient on long-term morphine treatment * Patient with known allergies to splint materials * Protected patient: adult under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative order * Pregnant woman * Patient hospitalized without consent * Patient already enrolled and participating in another clinical study
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What it tests

  • Intervention A
  • Intervention B
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Where

1 site
Clinique Jouvenet
Paris, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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