Пилотный этап SINEFIX-2022
Предпродажное клиническое исследование Inovedis SINEFIX
Shoulder pain is one of the most commonly reported musculoskeletal complaints, which negatively affects upper limb use, night rest, daily life activities, work, sports performance and autonomy. Rotator cuff disease represents the most common cause of shoulder pain and it is responsible for up to 70% of all shoulder related visits to clinicians. Its incidence furthermore is expected to grow as the population ages. A wide range of conditions are included under the umbrella term of rotator cuff disease, including rotator cuff tendinopathy, subacromial bursal pathology, and partial-thickness or full-thickness rotator cuff tears (RCTs). The latter ones, i.e. rotator cuff tears, form the indications for which the test devices, the SINEFIX implant and instruments, are intended.
Despite the high prevalence of this condition, the pathophysiology and healing potential are not well understood, making the condition challenging to predictably treat in some patient populations. RCTs may occur in young people as a consequence of trauma (e.g. acute shoulder dislocation), however RCTs typically present in middle-aged or elderly people and cannot always be attributed to precipitating events or trauma. Instead, they can be attributed to degenerative processes, and are therefore referred to as degenerative RCTs.
For RCTs, treatment options include both surgical and non-surgical (conservative) procedures.
In this context, the SINEFIX implant and instruments were developed to treat adult patients with rotator cuff lesions of size up to 2 cm through arthroscopic reconstruction.
Обзор исследования
Статус
Вмешательство/лечение
Тип исследования
Регистрация (Действительный)
Фаза
- Непригодный
Контакты и местонахождение
Места учебы
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Tübingen, Германия, 72074
- Orthopädisch Chirurgisches Centrum (OCC)
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
- Patient indicated for surgical repair of the rotator cuff tear according to current guidelines
- Patient aged 18 years or older
- Up to 2 cm tear size of supraspinatus, infraspinatus (medio-lateral)
- Up to 2 cm tear size of supraspinatus, infraspinatus (anterior-posterior)
Exclusion Criteria:
- Subject has had previous rotator cuff, arthroplasty or fracture procedures on the operative shoulder
- History of alcoholism, drug abuse, psychological or other emotional problems likely to interfere with participation in the study follow-up schedule and assessments
- Inflammatory arthropathies
- Subject with a contraindication/non-compliance for MRI examination
- Subject 's unwillingness to undergo surgical rotator cuff repair, participate in post-operative rehabilitation program, and / or adhere to follow up schedule
- Pregnant and breastfeeding woman
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Н/Д
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Экспериментальный: SINEFIX
Rotator cuff repair with the SINEFIX implant, using the SINEFIX instruments |
Treatment of rotator cuff lesions of size up to 2 cm using the SINEFIX implant and instruments |
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Healing integrity
Временное ограничение: 3 months post operation
|
Healing integrity will be assessed with the MRI by evaluating the visibility of the tendon underneath the implant (yes/no) |
3 months post operation
|
|
Re-tear rate
Временное ограничение: 3 months post operation
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Re-tear rate will be assessed with MRI |
3 months post operation
|
|
Dislocation of the implant
Временное ограничение: 3 months post operation
|
Presence of dislocation of the implant will be assessed with MRI (yes/no) |
3 months post operation
|
|
Bursitis
Временное ограничение: 3 months post operation
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Presence of bursitis will be assessed with MRI (yes/no) |
3 months post operation
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Surgery time
Временное ограничение: Immediately post procedure
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The total procedure duration will be recorded as the surgery time |
Immediately post procedure
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Usability and workflow assessment
Временное ограничение: Immediately post procedure
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Usability and workflow assessment will be evaluated after each intervention through a practitioner's questionnaire covering different aspects of the implant and instruments |
Immediately post procedure
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Functional and clinical outcome after rotator cuff repair
Временное ограничение: At 6 months, 1 and 2 years follow-up
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Functional and clinical outcome after rotator cuff repair will be assessed using the total Constant Murley score, which ranges from 0 (worst outcome) to 100 (best outcome) |
At 6 months, 1 and 2 years follow-up
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|
Functional and clinical outcome after rotator cuff repair as compared with baseline
Временное ограничение: At 6 months, 1 and 2 years follow-up
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Functional and clinical outcome after rotator cuff repair will be assessed using the change of the total Constant Murley score (range 0-100) as compared to baseline |
At 6 months, 1 and 2 years follow-up
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Shoulder function after rotator cuff repair (subjective evaluation)
Временное ограничение: At 10 weeks, 6, 12, and 24 months
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Shoulder function after rotator cuff repair (subjective evaluation) will be assessed through the Subjective Shoulder Value (SSV) which ranges from 0% to 100% (best outcome) |
At 10 weeks, 6, 12, and 24 months
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Shoulder function after rotator cuff repair (physical examination-active external rotation)
Временное ограничение: At 10 weeks, 6, 12, and 24 months
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Shoulder function after rotator cuff repair (physical examination) will be assessed through a physical examination with assessment of range of motion for active external rotation (range 0°-90°) |
At 10 weeks, 6, 12, and 24 months
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Shoulder function after rotator cuff repair (physical examination-active anteversion)
Временное ограничение: At 10 weeks, 6, 12, and 24 months
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Shoulder function after rotator cuff repair (physical examination) will be assessed through a physical examination with assessment of range of motion for active anteversion (0°-180°) |
At 10 weeks, 6, 12, and 24 months
|
|
Healing integrity
Временное ограничение: At 6, 12, and 24 months
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Healing integrity will be assessed with the MRI by evaluating the visibility of the tendon underneath the implant (yes/no) |
At 6, 12, and 24 months
|
|
Re-tear rate
Временное ограничение: At 6, 12, and 24 months
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Re-tear rate will be assessed with MRI |
At 6, 12, and 24 months
|
|
Dislocation of the implant
Временное ограничение: At 6, 12, and 24 months
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Presence of dislocation will be assessed with MRI (yes/no) |
At 6, 12, and 24 months
|
|
Bursitis
Временное ограничение: At 6, 12, and 24 months
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Presence of bursitis will be assessed with MRI (yes/no) |
At 6, 12, and 24 months
|
|
Complications
Временное ограничение: During the follow up time (up to 24 months)
|
Complications will be systematically reported. Complications of particular interest for the purpose of the study are neurological problems, bleeding, impaired wound healing, infection and frozen shoulder. |
During the follow up time (up to 24 months)
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Patient satisfaction
Временное ограничение: At 10 weeks, 6, 12, 24 months
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The patient will be asked to rate his/her satisfaction with outcome of the surgical repair (0=completely unsatisfied, 1=unsatisfied, 2=satisfied, 3=completely satisfied) |
At 10 weeks, 6, 12, 24 months
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Safety endpoint
Временное ограничение: During the intervention and the follow up time (up to 24 months)
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Safety of the device will be evaluated by systematically reporting device deficiencies (DDs), adverse events (AEs) and serious adverse events (SAEs) and by monitoring the frequency and incidence of these events |
During the intervention and the follow up time (up to 24 months)
|
Соавторы и исследователи
Спонсор
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- SINEFIX-2022
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .