挪威软骨项目——一项双盲随机对照试验的研究方案,该试验比较关节镜下微骨折术与关节镜下清创术治疗膝关节局灶性软骨缺损的疗效。
Norwegican Cartilage Project - a study protocol for a double-blinded randomized controlled trial comparing arthroscopic microfracture with arthroscopic debridement in focal cartilage defects in the knee.
作者信息
Aae Tommy Frøseth, Randsborg Per-Henrik, Breen Anne Berg, Visnes Håvard, Vindfeld Søren, Sivertsen Einar Andreas, Løken Sverre, Brinchmann Jan, Hanvold Heidi Andreassen, Årøen Asbjørn
机构信息
Department of Orthopedic Surgery, Kristiansund Hospital, Kristiansund, Norway.
Department of Orthopedic Surgery, Akershus University Hospital, Lørenskog, Norway.
出版信息
BMC Musculoskelet Disord. 2016 Jul 16;17:292. doi: 10.1186/s12891-016-1156-y.
BACKGROUND
Focal lesions to the articular cartilage in the knee might have demolishing consequences to the knee. There exists a wide range of possible surgical procedures targeting these injuries, however no significant differences have been found between these procedures. This may support that the improvement is a result of rehabilitation, and not the surgery itself. Arthroscopic microfracture (MF) treatment has gained popularity, and has become the treatment of choice in patients with knee cartilage defects globally. In this study we want to increase knowledge, both clinical and economic, about arthroscopic microfracture (AF) compared to arthroscopic debridement (AD) and physical rehabilitation both in the short run, and in the long run.
METHODS/DESIGN: To compare arthroscopic microfracture with arthroscopic debridement and physiotherapy for the treatment of focal cartilage lesions in the knee, a long-term, double-blinded, randomized controlled multicenter trial will be conducted. A total of 114 men and non-pregnant women with a symptomatic focal full thickness cartilage lesion in the knee less than 2 cm2 will be included in the study. The two treatment allocations will receive identical rehabilitation, which is made up of 3 phases: accommodation, rehabilitation and return to activity. Follow up is 24 months, where all will be invited to participate in late follow ups after 5 and 10 years. The Knee Injury and Osteoarthritis Outcome Score (KOOS) knee-related quality of life (QoL) subscore is the primary endpoint. Clinical parameters, questionnaires and radiologic modalities (Magnetic Resonance Imaging (MRI) and x-ray) will be used as secondary endpoints.
DISCUSSION
This is an ongoing multicenter study with a high level of evidence to compare arthroscopic microfracture with arthroscopic debridement and physiotherapy for the treatment of isolated symptomatic full thickness cartilage lesions in the knee joint.
TRIAL REGISTRATION
ClinicalTrials.gov ID: NCT02637505 (December 15, 2015).
背景
膝关节软骨的局灶性损伤可能会对膝关节造成严重后果。针对这些损伤存在多种可能的外科手术方法,但这些方法之间未发现显著差异。这可能支持改善是康复的结果,而非手术本身。关节镜下微骨折(MF)治疗已受到欢迎,并已成为全球膝关节软骨缺损患者的首选治疗方法。在本研究中,我们希望增加关于关节镜下微骨折(AF)与关节镜下清创术(AD)以及物理康复在短期和长期内的临床和经济方面的知识。
方法/设计:为比较关节镜下微骨折与关节镜下清创术及物理治疗对膝关节局灶性软骨损伤的治疗效果,将进行一项长期、双盲、随机对照多中心试验。共有114名有症状的膝关节局灶性全层软骨损伤面积小于2平方厘米的男性和非孕女性将被纳入研究。两种治疗组将接受相同的康复治疗,康复治疗由三个阶段组成:适应期、康复期和恢复活动期。随访时间为24个月,所有患者将被邀请在5年和10年后参加后期随访。膝关节损伤和骨关节炎疗效评分(KOOS)中与膝关节相关的生活质量(QoL)子评分是主要终点。临床参数、问卷和放射学检查方法(磁共振成像(MRI)和X线)将用作次要终点。
讨论
这是一项正在进行的多中心研究,具有较高的证据水平,用于比较关节镜下微骨折与关节镜下清创术及物理治疗对膝关节孤立性有症状全层软骨损伤的治疗效果。
试验注册
ClinicalTrials.gov标识符:NCT02637505(2015年12月15日)。