跳至主要内容
临床试验/NCT05342441
NCT05342441招募中不适用

Optimizing GRAft SElection for ACL Reconstruction (GRASE-ACL Trial) - a Three-armed Randomized Controlled Trial

Hvidovre University Hospital2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2022年5月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
150
试验地点
2
主要终点
Rate of Torque Development - Limb Symmetry Index (RFD-LSI).

研究概览

简要总结

Purpose:

To investigate the differences between the three most common methods for reconstruction of the anterior cruciate ligament (ACL), to support the development of the best method for the individual patient.

Main research area: ¨ Sports Orthopedic Surgical research.

State of the art:

Every year in Denmark 2500 patients receive surgical reconstruction surgery to replace a ruptured ACL. Many patients experience a decline in knee function and 4-12% suffer a new ACL rupture within 5 years. According to data from the Danish ACL register, three methods of reconstruction are most prevalent, but with large variation between hospitals. This indicates lack of consensus on optimal surgical procedure.

Design:

Assessor-blinded randomized controlled study. 150 patients aged 18-40 with ruptured ACL are allocated to reconstruction with tendon(s) harvested from either the semitendinosus and gracilis, or the patella tendon, or the quadriceps tendon. Patient follow-up will be conducted preoperatively and 1, 6, 12, 24 months postoperatively.

Primary technologies and outcomes:

  • Patient-reported knee-joint function, quality of life and donor-site morbidity is obtained with standardized questionnaires. Primary outcome is subjective knee function with the International Knee Documentation Committee evaluation form (IKDC)
  • Instrumented analysis of knee-joint coordination and neuromuscular control including 3-D motion capture and electromyography (EMG) during single leg jumps, landings and change-of-direction. Measurement of maximal explosive muscle power in knee extension and flexion. Primary outcome is relative difference between injured and healthy leg in rate of force development (RFD-LSI).
  • Standard clinical knee examination of range of motion and instrumented examination of knee-joint stability.
  • Magnetic Resonance Imaging (MRI) of the thigh muscles for examination of muscle morphology.

The trial is designed for publication in three primary publications

  1. - Patient reported effect of graft choice in ACL reconstruction
  2. - Biomechanical effect of graft choice in ACL reconstruction
  3. - Clinical effect of graft choice in ACL reconstruction

Additional secondary publications are in the pipeline. Reference to primary protocol and results will always be emphasized in secondary publication to ensure methodological transparency.

详细描述

Purpose:

The aim of this randomized controlled trial is to investigate the effect of graft choice in anterior cruciate ligament (ACL) reconstruction surgery, primarily from a patient-centered as well as a novel biomechanical perspective; and secondly from a clinical and muscle morphological perspective.

The study compares the three most common methods for ACL reconstruction: autograft harvested from the m. quadriceps tendon (QT), the hamstring tendons (ST/Gr), and the patella tendon (BPTB).

By applying this 360° scientific approach, it is the hope to improve the possibilities for a much-needed evidence-based and individualized treatment of ACL ruptures.

Objectives and hypotheses:

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
Single (Outcomes Assessor)

盲法说明

Outcome assessors are blinded to group allocation. Before each patient visit, tape will be placed on possible scars to hide donor graft site. Given the nature of the intervention, blinding of patients and surgeons is not feasible.

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Rate of Torque Development - Limb Symmetry Index (RFD-LSI).

时间窗: 12 months follow up

Hamstring and quadriceps rate of torque development in the injured/operated leg compared to the healthy leg, expressed in percentage with 100% being full symmetry and the best outcome.

International Knee Documentation Committee score (IKDC).

时间窗: 12 months follow up.

Patient-reported knee function based on a questionnaire, expressed on a scale form 0-100 with 100 being the best outcome.

次要结局

  • Knee laxity(Baseline, 6, and 12 months.)
  • Hamstring muscles retraction(At 12 months follow up.)
  • Donor site discomfort.(Baseline, 6, 12, and 24 months follow up.)
  • Rate of torque Development - Limb Symmetry Index (RFD-LSI).(Baseline, 1, 6, and 24 months follow up.)
  • Muscle cross sectional area(At 12 months follow up.)
  • Return to sport questionnaire.(Baseline, 6, 12 and 24 months follow up.)
  • Knee and hip angles.(Baseline, 6, and 12 months follow up.)
  • Number of patients undergoing revision surgery due to graft failure.(Baseline, 12, and 24 months follow up.)
  • Number of patients experiencing re-rupture of the operated ACL.(Baseline, 12, and 24 months follow up.)
  • Workability questionnaire(Baseline, 1, 6, 12, and 24 months follow up.)
  • Neuromuscular control.(Baseline, 6, and 12 months follow up.)
  • International Knee Documentation Committee score (IKDC).(Baseline, 1, 6, and 24 months follow up.)
  • Patient Acceptable Symptom State questionnaire (PASS)(Baseline, 12, and 24 months.)
  • Knee and hip moments.(Baseline, 6, and 12 months follow up.)
  • Number of patients experiencing rupture of the contralateral ACL.(Baseline, 12, and 24 months follow up.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kristoffer Barfod

Consultant, MD, PhD, Associate Professor

Hvidovre University Hospital

研究点 (2)

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