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临床试验/NCT03956381
NCT03956381已完成不适用

A Study to Demonstrate the Accuracy of Femoral Neck Resection Compared to the Pre-operatively Selected OPS™ Plan in Total Hip Arthroplasty.

Corin1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2019年4月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Corin
入组人数
55
试验地点
1
主要终点
Accuracy of the final osteotomy level compared to the selected OPS™ plan preopertively.

研究概览

简要总结

The primary objective of this study is to determine the accuracy of the Optimized Positioning System (OPS™) planning and delivery tools using different types of surgical approaches.

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 two surgeons using different prosthesis combinations and surgical approaches. A total number of 40 participants 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 post-operative study hip related complications to be recorded. Once this has been completed, participants will be routinely followed-up by their orthopaedic surgeon as required in accordance with 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

入选标准

  • Patients who understand the conditions of the study and are willing to return to the clinical site at 6 weeks post-operatively.
  • Patients of either gender who are between 21-85 years inclusive.
  • Patients with a diagnosis of osteoarthritis, rheumatoid arthritis or osteonecrosis 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 whose insurance will not cover the cost of the pre-operative CT and functional x-ray imaging required for use of the OPS system.
  • 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 preopertively.

时间窗: 6 weeks post-op (+/- 2 weeks)

Accuracy of the final osteotomy level compared to the selected OPS™ plan (+ or - 3mm). Two standard of care post-operative x-rays taken at 6 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 preoperatively (± 1 size)(Immediate postoperative)
  • Comparison of the acetabular cup size implanted compared to the selected OPS™ Plan preoperatively.(Immediate postoperative)
  • Comparison of the femoral head size implanted compared to the selected OPS™ Plan preoperatively.(Immediate postoperative)
  • Measurement of any change in Leg length/ femoral head height compared to the preoperative OPS™ Plan (± 5mm).(6 weeks post-op (+/- 2 weeks))
  • Comparison of the acetabular cup orientation to the selected OPS™ Plan.(6 weeks post-op (+/- 2 weeks))

研究者

发起方
Corin
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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