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临床试验/NCT03184922
NCT03184922进行中(未招募)不适用

A Prospective, Randomised Study Investigating the Use of a Fixed Loop Versus an Adjustable Suspensory Loop in Anterior Cruciate Ligament Reconstruction - a Comparison of Clinical and Functional Outcome

Royal Devon and Exeter NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 165 人开始时间: 2017年7月5日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
165
试验地点
2
主要终点
The assessment of knee joint stability via a comparison of left and right sided anterior tibial translation

研究概览

简要总结

Study Aims and Objectives:

To investigate the following null hypothesis: that there is no difference in clinical and functional outcome when comparing outcomes of Anterior Cruciate Ligament (ACL) reconstruction when comparing femoral side graft fixation with either a fixed versus an adjustable suspensory loop system.

The research team will achieve this aim by:

  • Enrolling 150 patients into this study over a period of 2 years and 8 months
  • Carrying out a prospective randomised study looking at the subject matter over a period of 5 years and 8 months
  • Analysing patients functional status pre and post-surgery using patient generated questionnaires
  • Quantitatively measuring knee joint laxity using the KT1000 testing device at the 3, 6 and 12 month post-surgery time frames
  • Collating the data received into a spread sheet for analysis by a professional statistician.

It is not uncommon to tear the anterior cruciate ligament (ACL) particularly during sporting activities. Younger and sportier patients will often have this ligament reconstructed so as to allow them to return to sport with a stable knee joint that they feel they can trust.

Various surgical techniques exist to perform ACL reconstruction. In Exeter, the favoured technique is to reconstruct the ligament by taking two of the hamstring tendons from the back of the knee and creating a graft with these, passing them through a bony tunnel to replace the torn ACL. On the shin bone side of the knee the graft is fixed in place using a screw. On the thigh bone side, the graft is attached to a device known as a suspensory loop.

The length of the graft and the length of the tunnel in the thigh bone vary from patient to patient. It is important to get a good length of the graft material in both the shin and thigh bones so as to give the best chance of the graft attaching to the surrounding bone. With the fixed loop system, once the metal button attached to the outer thigh bone is in place, the length of the loop cannot be adjusted. Thus the amount of hamstring graft in either end of the bony tunnel cannot be changed. One potential advantage of an adjustable loop system is that the amount of graft in either end of the bone tunnel can be altered to ensure sufficient graft is accurately placed.

The research team are planning to run this study to identify which type of loop system gives the best outcome for patients, examining the results in different ways including questionnaires to measure how well the patients feel their knee is performing, and specific tests to measure knee function.

If patients consent to be in the study, they will be randomly allocated to receive one of the 2 ACL reconstruction options above and their progress monitored for 2 years after the operation. All aspects of surgical care will be as routine practice apart from the decision to fix the graft to the thigh bone with an adjustable or fixed suspensory loop.

详细描述

Research Question:

In the treatment of patients requiring anterior cruciate ligament (ACL) reconstruction, is there any difference in clinical and functional outcomes for patients when comparing femoral side graft fixation using a fixed loop versus an adjustable suspensory loop system?

Study Aims and Objectives:

  1. To investigate the following null hypothesis: that there is no difference in clinical and functional outcome when comparing outcomes of ACL reconstruction when comparing the use of a fixed versus an adjustable suspensory loop system.
  2. To identify the optimal surgical technique for patients requiring ACL reconstruction surgery.

The research team will achieve these aims by:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

  1. The patients will be informed they will not be told which arm of the study they are allocated to.
  2. The outcomes assessor for the KT1000 will be a physiotherapist not a surgeon and will not be told which type of surgery the patient has undergone

入排标准

年龄范围
16 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Isolated ACL deficient knee without other ligament injury
  • Patients who have a small meniscal tear that requires flap excision during the ACL surgery can be included in the study-see

排除标准

  • Patient has signed an ethics committee approved consent form
  • Surgery to be performed at either at The Royal Devon and Exeter Hospital or Sidmouth Hospital.
  • Patient is willing and able to comply with postoperative scheduled clinical and functional evaluations and rehabilitation
  • Patients undergoing ACL reconstruction using hamstring autograft
  • Exclusion Criteria:
  • Patients <16 years old
  • Refusal to consent to participate in the study
  • Previous knee surgery or serious knee injuries in the operative knee
  • Obvious clinical knee malalignment-i.e. visible on clinical examination
  • Multi ligament knee injuries.
  • Moderate to severe degenerative changes present within the knee joint.
  • If a simultaneous sub-total meniscectomy involving 50% or more of the meniscus has to be performed
  • Patients who also have a postero-lateral corner injury
  • Patient has a neuromuscular or neurosensory deficiency
  • Pregnancy

结局指标

主要结局

The assessment of knee joint stability via a comparison of left and right sided anterior tibial translation

时间窗: 12 months after surgery

Anterior tibial translation will be assessed using the KT1000 device using a students t-test or a non-parametric equivalent if the data is not normally distributed e.g. the Mann- Whitney u test to compare the groups. The Minimal Clinically Important Difference between the groups will be 0.6mm above the acceptable threshold of 3mm

次要结局

  • An assessment of Functional outcome (4) using the results of the International Knee Documentation Committee (IKDC) subjective questionnaire(6 months after surgery)
  • IKDC subjective knee questionnaire(24 months after surgery)
  • Tegner activity scale: Functional outcome 11(12 months after surgery)
  • An assessment of Functional outcome (2) using the results of the Knee Osteo-Arthritis Outcome Score (KOOS)(12 months after surgery)
  • Lysholm knee score: Functional outcome 7(6 months after surgery)
  • Lysholm knee score: Functional outcome 9(24 months after surgery)
  • Tegner activity scale: Functional outcome 10(6 months after surgery)
  • Tegner activity scale: Functional outcome 13(24 months after surgery)
  • An assessment of Functional outcome (1) using the results of the Knee Osteo-Arthritis Outcome Score (KOOS)(6 months after surgery)
  • An assessment of Functional outcome (3) using the results of the Knee Osteo-Arthritis Outcome Score (KOOS)(24 months after surgery)
  • Lysholm knee score: Functional outcome 8(12 months after surgery)

研究者

发起方
Royal Devon and Exeter NHS Foundation Trust
申办方类型
Other
责任方
Sponsor

研究点 (2)

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