The Effects of Remnant-Preserving Anterior Cruciate Ligament Reconstruction on Proprioception and Functionality
2022年5月18日 更新者：Özgül Öztürk、Acibadem University
Anterior cruciate ligament (ACL) reconstruction is a frequently performed surgical procedure to stabilize the knee joint biomechanically.
At the same time, one of the goals is to improve clinical outcomes and return the patient to their daily life as early and ready as possible, as well as to sports activities.
Remnant-preserving anterior cruciate ligament reconstruction is one of the reconstruction approaches that aim to achieve these goals earlier and more safely than the standard surgical procedure.
However, there is no consensus in the literature regarding the effects of remnant-preserving ACL reconstruction on clinical outcomes and its superiority over the standard surgical procedure.
Therefore, the aim of our study is to compare the proprioception and functionality of patients who underwent ACL reconstruction with the remnant-preserving approach, by classifying them according to stump size.
研究概览
研究类型
观察性的
注册 (实际的)
65
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
-
-
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Istanbul、火鸡
- Marmara University Department of Physiotherapy and Rehabilitation
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 45年 (成人)
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients who were underwent remnant-preserving anterior cruciate ligament reconstruction
描述
Inclusion Criteria:
- Aged between 18 - 45 years,
- Anatomical single-bundle ACL reconstruction with antero-medial portal technique using hamstring autograft due to a full-thickness ACL tear,
- Endobutton technique was used for femoral fixation,
- Has not had any trauma or surgery on the non-operated knee,
- Patients with a follow-up period of at least 12 months after surgery.
Exclusion Criteria:
- Fracture of lower extremity, posterior cruciate ligament, inner and outer lateral ligament tears accompanying anterior cruciate ligament tear,
- Patients who have undergone previous surgery on the targeted knee,
- Have a revision anterior cruciate ligament reconstruction,
- Having a history of knee joint arthritis (osteoarthritis, inflammatory arthritis),
- Have a neurological disease,
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
Anterior Cruciate Ligament Reconstruction
|
Proprioception assessment, functionality assessment
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proprioception assessment
大体时间：1 day
|
Biodex® System Pro 4 (Biodex Cor.
Shirley NY, USA) device will be used to evaluate the proprioception of the knee joint.
The subjects will be asked to sit on the isokinetic dynamometer device with the knee joint in 90º flexion.
The proprioception sense of the operated and non-operated knees will be measured at three different angles of 20º, 50º and 70º.
Before the test, the procedures during the test such as knee flexion-extension, target angle and target angle recall will be assessed when eyes are open and closed.
The test will be explained and actively demonstrated to all subjects before starting the assessment.
During the test, the target angle will be displayed by the device and the limb will be held in this position for 10 seconds.
|
1 day
|
|
The Lysholm Score
大体时间：1 day
|
The Lysholm Scale is used to evaluate the functionality of the knee joint, has a score between 0 and 100 points.
In this scoring system, a higher score indicates a better functionality.
|
1 day
|
|
Single Leg Hop Test
大体时间：1 day
|
Single leg forward hop test will be used to determine the functional performance level of the patient depending on the dynamic stability of the knee.
The participant will be asked to stand on the leg to be tested at the starting point of the tape measure, whose toes are fixed to the floor, and to jump forward and as far as possible on the leg to be tested, along the tape measure line without losing balance.
If the balance is disturbed and the foot touches the ground, the test will be repeated.
There will be a one-time trial to learn the test.
The test will be repeated 3 times with a 30-second rest period in between.
|
1 day
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年10月1日
初级完成 (实际的)
2022年5月5日
研究完成 (实际的)
2022年5月10日
研究注册日期
首次提交
2021年9月16日
首先提交符合 QC 标准的
2021年9月16日
首次发布 (实际的)
2021年9月27日
研究记录更新
最后更新发布 (实际的)
2022年5月20日
上次提交的符合 QC 标准的更新
2022年5月18日
最后验证
2022年5月1日
更多信息
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