跳至主要内容
临床试验/NCT07028476
NCT07028476招募中不适用

NPS-LDA - New Care Pathway Using Automated Dynamic Laximetry

University Hospital, Angers3 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年3月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
3
主要终点
EQ-5D-5L questionnaire

研究概览

简要总结

Today, in the event of a knee sprain with suspected cruciate ligament damage, magnetic resonance imaging (MRI) is generally prescribed to confirm or refute the diagnosis and assess its severity. Once the MRI has been performed, the patient's care is organized by the doctor of his or her choice, depending on the diagnosis.

Previous studies have shown that Automated Dynamic Laximetry (ADL) performs identically to MRI in helping to diagnose a knee sprain as a complementary examination and in assessing its severity. Performing LDA at the start of the patient's care pathway, i.e. immediately after the emergency room visit for a suspected severe sprain, could bring significant benefits by shortening the diagnostic confirmation time and consequently the immobilization period, and by reducing the cost of care compared with the conventional MRI-based care pathway. The new LDA-based care pathway would enable MRI to be reserved for very specific cases, such as the scheduling of surgery for suspected meniscus or osteochondral lesions, as currently recommended by the HAS.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patient admitted to an emergency department participating in the study
  • •Age ≥ 18 years
  • •Consulted following knee trauma and whose clinical examination leads to the suspicion of a partial or complete ACL lesion without bone fracture (supporting radiograph).
  • •Signed consent to participate in the study
  • •Affiliated to a social security scheme

排除标准

  • •Contraindication to MRI (pacemaker fitted before 2010) or LDA;
  • •Indication for emergency or semi-emergency trauma surgery (within 3 weeks: suspected unstable meniscal lesion, fracture, etc.).
  • •Impossible follow-up or patient's refusal of follow-up in the investigating center's sports medicine department;
  • •Poor understanding of the French language
  • •Pregnant (known or suspected pregnancy), breast-feeding or parturient woman;
  • •Person deprived of liberty by judicial or administrative decision;
  • •Person under compulsory psychiatric care;
  • •Person subject to a legal protection measure
  • •Person unable to give consent

研究组 & 干预措施

Pds-IRM

Experimental

干预措施: MRI (Procedure)

Pds-LDA

Active Comparator

干预措施: Automated Dynamic Laximetry (Procedure)

结局指标

主要结局

EQ-5D-5L questionnaire

时间窗: Inclusion, 1 month, 3 months, 6 months and 12 months

The EQ5D-5L question listings are designed to analyze quality of life across 5 themes (mobility, personal autonomy, daily activities, pain/discomfort, anxiety/depression and health assessment).

KOOS questionnaire

时间窗: 3 months

The Knee Injury and Osteoarthritis Outcome Score (KOOS) is used to assess immediate and long-term patient outcomes following knee injury. Five outcomes are assessed by the self-administered KOOS: pain, symptoms, activities of daily living, sports and recreational function, and knee-related quality of life. KOOS meets basic standards for outcome measures and can be used to assess the evolution of the knee injury and the effectiveness of treatment. KOOS is patient-administered, has an easy-to-use format and takes around 10 minutes to complete.

次要结局

  • KOOS questionnaire(Inclusion, 1 month, 3 months and 12 months)
  • Tegner activity scale(Inclusion, 1 month, 3 months and 12 months)
  • Cost per QALY gained(12 months)
  • Time frame for therapeutic management(inclusion and start of therapeutic management)
  • Time to First Return to Sporting Activity(12 months)
  • Time to Return to Work(12 months)
  • Average recovery time to pre-sprain level:(12 months)
  • budgetary impact(12 months)

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验