Radiographic and Clinical Evaluation of Surgical Treatment for Cervical Deformity: A Multi-Center Study 2.0
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Surgical intervention.
- Кому может быть актуально
- Состояния в реестре: Cervical Deformity. Базовые параметры: от 18 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- США
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Prospective Radiographic and Clinical Evaluation of Surgical Treatment for Cervical Deformity: A Multi-Center Study 2.0
Обзор
Multi-center, prospective, non-randomized study to evaluate outcomes of surgically treated patients with adult cervical spinal deformity.
Подробное описание
Adult cervical deformity (ACD) is an uncommon but potentially severely debilitating condition with a broad range of causes that include but are not limited to spondylosis, inflammatory arthropathy, trauma, infection, iatrogenic, neoplastic, congenital, and neuromuscular processes. In general, sagittal plane deformities typically produce kyphosis, and coronal plane deformities result in scoliosis. Cervical kyphotic deformities are most commonly encountered in the setting of prior surgical destabilization, while cervical scoliosis is most commonly associated with congenital and neuromuscular conditions.
Cervical kyphosis may be progressive and can result in neurological symptoms, including myelopathy. The most severe forms, such as those associated with spondylotic arthropathies, can produce "chin-on-chest" deformity, which can compromise horizontal gaze, swallowing, and breathing. Even in the absence of these conditions, cervical deformity is often associated with pain and functional disability. For adult thoracolumbar deformities, substantial efforts have been made to characterize clinical presentations, develop standardized classification systems, define optimal treatment approaches, describes operative complication rates, and to present structured clinical outcomes. However, despite the potential for profound impact of cervical deformity on function and health-related quality of life, there remains a remarkable paucity of high-quality studies that address these complex conditions.
Health professionals providing nonoperative and surgical care for these patients are left to make important treatment decisions based on a combination of personal experience, anecdotal experience of colleagues and experts, and relatively small, often single-surgeon or single-center, retrospective case reports or case series in the literature. Recent systematic reviews have high-lighted the lack of studies relevant to cervical deformity and have failed to identify any prospective studies.
The International Spine Study Group (ISSG) consists of orthopedic and neurological spine surgeons with a practice emphasis on spinal deformity patients. These surgeons, from 12 busy surgical centers, meet regularly to design and perform clinical research focused on spinal deformity, including successful prospective enrollment of more than 1,000 adult thoracolumbar deformity patients into the ISSG database. This group has a proven track record and regularly presents a substantial number of abstracts to the major spine meetings and has an extensive publication record.
The ISSG members have currently enrolled more than 150 patients into the first generation prospective cervical deformity database and have produced approximately 50 abstracts and more than 25 manuscripts to date with the resulting data. The group has learned extensively from this first-generation database, but there is much yet to learn, as the literature remains relatively sparse on the topic of adult cervical deformity. Based on what we have learned from the first generation database; we have substantially modified the inclusion criteria for this second generation database. In addition, several new outcomes measures and functional assessments will be collected at baseline and follow-up intervals as part of this current proposal.
The resources of the ISSG offer an unprecedented opportunity to create a prospectively collected multicenter database of cervical deformity patients that includes standardized health-related quality of life measures at baseline and regular follow-up, clinical and surgical parameters, and complications. The database and questionnaires have been carefully redesigned based on what we have learned in order to better collect data that will help to clarify many of the unresolved issues that are important for the care of cervical deformity patients. This project has substantial potential to significantly impact the field of cervical deformity and the care of deformity patients beyond what we have already been able to accomplish based on the first generation cervical deformity database. Herein we propose the second iteration for this project that promises to further advance our evolving understanding of these complex deformities.
Вмешательства
- Процедура Surgical intervention
Surgical interventions will be patient specified by treating surgeon.
Первичные конечные точки
- Pain Numeric rating scale (NRS) - Headaches [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Pain Numeric rating scale (NRS) - Neck [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Pain Numeric rating scale (NRS) - Upper extremity [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Pain Numeric rating scale (NRS) - Lower extremity [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Pain Numeric rating scale (NRS) - Back [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Neck Disability Index (NDI) [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Veterans RAND 12 Item Health Survey (VR-12) [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Anxiety [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Depression [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
Вторичные конечные точки (6)
- EAT-10 [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Voice Handicap Index (VHI-10) [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Adverse evnts [Срок оценки: 3 months and 1, 2, 5 & 10 year post treatment]
- Edmonton Frail Scale [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- CHSF Frail Scale [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
- Dynamometer Hand Grip Strength test [Срок оценки: Change from Preop to 3 months, 6 months and 1, 2, 5 & 10 year follow-up]
Критерии участия
Критерии включения
- ≥18 years old at time of treatment
- Diagnosis of cervical deformity- must meet one or more of the following criteria:
- C2-C7 sagittal kyphosis (Cobb > 15 degrees)
- T1S-CL > 35o
- Segmental cervical kyphosis > 10 degrees between any 2 vertebra between C2-T1 or > 15 degrees across any 3 vertebra between C2-T1
- Cervical scoliosis > 10 degrees (Cobb angle must include end vertebra within the cervical spine)
- C2-C7 SVA > 4cm
- McGregor's slope > 20 degrees or CBVA > 25 degrees OR
- Planned Revision surgery for proximal junctional failure with an anticipated UIV in the cervical spine and an anticipated LIV in the thoracic or lumbar spine.
- Plan for surgical correction of cervical deformity in the next 6 months
- Willing to provide consent and complete study forms at baseline and follow-up intervals
- Upright AP/Lateral entire spine (EOS or 36")
- Upright AP/Lateral C spine ONLY IF C spine is not completely visible on entire spine films
- Flex/Ext lateral C spine. Admin may allow exceptions w/ valid documentation.
Критерии исключения
- Active spine tumor or infection
- Deformity due to acute trauma
- Unwilling to provide consent or to complete study forms
- Prisoner
- Pregnant or immediate plans to get pregnant
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
США · 16 центров
- Shiley Center for Orthopaedic Research and Education at Scripps Clinic — La Jolla
- University of California Davis, Department of Orthopedic Surgery — Sacramento
- University of California-San Francisco Medical Center — San Francisco
- Denver International Spine Center, Rocky Mountain Hospital for Children and Presbyterian S — Denver
- Rush University, Department of Neurosurgery — Chicago
- University of Kansas Medical Center, Department of Orthopedic Surgery — Kansas City
- Leatherman Spine Center, Department of Orthopedic Surgery — Louisville
- Johns Hopkins University, Department of Neurological Surgery — Baltimore
- … и ещё 8 центров
Идентификаторы
NCT: NCT04194996 · 2131