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临床试验/NCT07819929
NCT07819929尚未招募不适用

Mid-term Postoperative Clinical Evaluation of Patients Undergoing Anterior Cruciate Ligament (ACL) Reconstruction Using the Over-The-Top Technique, Fixed With Metal Staples or Soft Anchors

Stefano Zaffagnini1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
46
试验地点
1
主要终点
KT-1000

研究概览

简要总结

Anterior cruciate ligament (ACL) reconstruction is a widely performed procedure aimed at restoring knee stability and enabling return to sports activities. The Over-The-Top (OTT) technique is a well-established option, particularly in complex and revision cases, due to its ability to provide both anteroposterior and rotational stability. Long-term studies have reported favorable clinical outcomes, with low failure rates.

Graft fixation is an important technical aspect that may influence postoperative outcomes. Traditionally, the OTT technique has been performed using metal staples, which provide reliable primary fixation but may cause local complications and sometimes require subsequent removal due to pain or discomfort.

More recently, suture-based fixation devices, such as Knee FiberTak anchors (Arthrex), have been introduced as a metal-free alternative. These devices allow graft fixation through high-strength sutures, providing stable graft-to-bone contact while minimizing bony invasiveness and hardware prominence.

The present study aims to evaluate the clinical, functional, and instrumental outcomes of ACL reconstruction using the OTT technique with graft fixation by suture anchors compared with traditional metal staples. Particular attention will be paid to postoperative knee stability, assessed using validated instruments (KT-1000 and KiRA), as well as failure rates, reoperations, and complications.

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
None

入排标准

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

入选标准

  • Patients of either sex, aged between 18 and 50 years at the time of surgery;
  • Patients with an isolated anterior cruciate ligament (ACL) injury, with or without associated meniscal lesions, scheduled for ACL reconstruction and meniscal treatment; .3 Patients whose contralateral knee has never undergone meniscectomy, ligament reconstruction, unicompartmental knee arthroplasty, or total knee arthroplasty;
  • 4. Patients who have signed the informed consent form.

排除标准

  • Patients with associated injury of the medial collateral ligament (MCL), lateral collateral ligament (LCL), posterolateral corner (PLC), or posterior cruciate ligament (PCL);
  • Patients with complete meniscal root tears, complete radial tears, or lateral meniscus oblique tears (LMORT);
  • Patients who underwent total or subtotal medial or lateral meniscectomy;
  • Patients with grade III-IV chondral lesions according to the Outerbridge classification identified at the time of surgery;
  • Patients who are unable to provide informed consent or who are unwilling to provide informed consent;
  • Patients with insufficient and/or compromised bone quality or quantity due to disease, infection, or previous implantation, such that adequate support and/or fixation of the devices cannot be ensured;
  • Patients with limited blood supply or a history of infections that could delay healing;
  • Patients with sensitivity to foreign materials.

研究组 & 干预措施

Soft anchors

Experimental

干预措施: ACL reconstruction using the Over-The-Top technique (Procedure)

Metal staples

Active Comparator

干预措施: ACL reconstruction using the Over-The-Top technique (Procedure)

结局指标

主要结局

KT-1000

时间窗: At least 24 months

The KT-1000 is a clinical-instrumental test widely used for the standardized assessment of patients undergoing anterior cruciate ligament (ACL) reconstruction. It provides an objective measurement of anterior-posterior knee laxity and is extensively used in both clinical practice and scientific research. The assessment is performed with the patient in a supine position, with the knee flexed to approximately 30° and supported on a dedicated device. The examiner applies a standardized anterior load to the tibia while stabilizing the femur, and the resulting anterior-posterior displacement is recorded by sensors positioned in contact with the patella and tibial tuberosity. The measurement does not have a predefined minimum or maximum value. Lower values indicate less anterior laxity and therefore better knee stability, whereas higher values indicate greater anterior laxity and worse knee stability.

次要结局

  • KiRA(At least 24 months)
  • IKDC standard evaluation form(At least 24 months)
  • Lysholm Knee Score(At least 24 months)
  • VAS(At least 24 months)
  • SF-12 (Short Form-12 Health Survey)(At least 24 months)
  • KOOS (Knee Injury and Osteoarthritis Outcome Score)(At least 24 months)
  • Tegner Score(At least 24 months)
  • Patient Satisfaction(At least 24 months)

研究者

发起方
Stefano Zaffagnini
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Stefano Zaffagnini

Full Professor Medicine and Surgery, University of Bologna

Istituto Ortopedico Rizzoli

研究点 (1)

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