A Study to Demonstrate the Accuracy of the Femoral Neck Resection Compared to the Selected OPS™ Plan Using the Direct Anterior Approach (DAA)
试验速览
- 阶段
- 不适用
- 发起方
- Corin
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Accuracy of the final osteotomy level compared to the selected OPS™ Plan
研究概览
简要总结
A prospective, non-randomized, single-center clinical study to determine the accuracy of a patient-specific instrument (OPS™) for delivering a planned femoral component anteversion and neck resection using a Direct Anterior Approach (DAA) in Total Hip Arthroplasy.
详细描述
Total Hip Replacement (THR) is the gold standard for treatment of severe arthritis of the hip as it relieves pain, restores function of the joint, and improves quality of life for patients. The restoration of hip mechanics can be influenced by the selected femoral stem design and also by choices made by the surgeon during the surgical implantation. The combination of femoral neck resection level and angle are key factors, particularly in cementless hip arthroplasty, in determining post-operative leg length and femoral anteversion. Historically, an estimation of prosthesis sizing and positioning has been made via a process of manual or digital templating either pre or intraoperatively using images of the implants positioned over the standard AP and lateral view hip x-rays taken in advance of surgery with generic instruments used during the surgery to execute the femoral head resection at the planned level. This process has a number of limitations. The OPS™ system utilizes detailed pre-operative imaging including a CT scan to generate a plan for the femoral neck resection level and angulation based on the anatomy of the individual patient. Following validation of this plan by the operating clinician, a patient specific femoral guide instrument is generated to help facilitate the reliable delivery of the planned resection intraoperatively. The purpose of this study will be to evaluate the use of the patient-specific femoral instrument in the hands of one surgeon using a protocol-specific choice of prosthesis combinations and one surgical approach. A total number of 100 subjects will be enrolled. Participants in this study will return for a single post-operative visit at 6 weeks to have x-rays taken and to enable any postoperative study hip-related complications recorded. Once this has been completed, participants will be routinely followed-up by their Orthopedic surgeon as required in accordance with the standard clinical practice.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 21 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who understand the conditions of the study and are willing to return to the clinical site at 2 weeks postoperatively.
- •Patients of either gender who are between 21-85 years (inclusive) at the time of consent.
- •Patients with a diagnosis of osteoarthritis (including post-traumatic osteoarthritis), rheumatoid arthritis or avascular necrosis and are considered by the Investigator to be clinically and medically suitable to undergo a primary total hip replacement.
- •Patients who meet the indications and none of the contraindications listed in the Instructions for Use (IFU) supplied by the manufacturer for the femoral stem and acetabular cup to be implanted.
- •Patients who meet the indications and none of the contraindications listed in the Instructions for Use (IFU) supplied by the manufacturer for OPS™ Femoral Plan and OPS™ Femoral Patient Specific Instruments.
排除标准
- •Patients who are unable to provide informed consent.
- •Patients who are unable to comply with all the required study procedures.
- •Patients who are currently involved in any personal injury litigation, medical-legal or worker's compensations claims.
结局指标
主要结局
Accuracy of the final osteotomy level compared to the selected OPS™ Plan
时间窗: 2 weeks post-op (1 - 4 weeks post-op window)
Accuracy of the final osteotomy level compared to the selected OPS™ Plan (+ or - 3 mm). Two standard of care postoperative x-rays taken at 2 weeks will be used to evaluate the positioning of the total hip prosthesis from the resultant level of resection of the femoral neck. This parameter will be measured in mm.
次要结局
- Comparison of the femoral stem size implanted compared to the selected OPS™ Plan(Immediate postoperative)
- Comparison of the acetabular cup size implanted compared to the OPS™Plan(Immediate postoperative)
- Comparison of the femoral head size implanted compared to the selected OPS™ Plan(Immediate postoperative)
- Measurement of any change in leg length / femoral head height compared to the preoperative OPS™ Plan(2 weeks post-op (1 - 4 weeks post-op window))
- Comparison of the acetabular cup orientation to the selected OPS™ Plan(2 weeks post-op (1 - 4 weeks post-op window))