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临床试验/NCT02275494
NCT02275494已完成不适用

The Influence of Leg Length Discrepancy After Total Hip Arthroplasty on Function and Quality of Life

Sundsvall Hospital0 个研究点目标入组 174 人开始时间: 2010年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
174
主要终点
WOMAC

研究概览

简要总结

Leg length discrepancy (LLD) is a complication of THA and may result in patient dissatisfaction, gait disorder, greater trochanter pain, low back pain. In the literature, LLD is reported to vary widely among studies e.g. 6 to 35 mm. However, the threshold at which a LLD is clinically important is still a matter of debate. The aim of this study was to determine the influence of non-corrected LLD after THA on patients' reported hip function and quality of life. This prospective cohort study was conducted at Sundsvall Teaching Hospital in Sweden after it was approved by the regional ethics committee at Umeå University (No. 07-052M and No. 12-287-32M). Between September 2010 and April 2013, all patients with unilateral primary osteoarthritis (OA) treated with THA were considered for inclusion. Informed consent was obtained from all patients. Patients with secondary OA, previous spinal, pelvic, or lower limb injuries or fractures were excluded.

The primary outcome measure was the Western Ontario and McMaster Universities Osteoarthritis (WOMAC) Index that measures functional outcome (ref). The secondary outcome measure was the EQ-5D and visual analogue scale (VAS) scale. Patients were assessed preoperatively and at follow-up at 1 year postoperatively. The posterolateral approach was used in all operations. LLD was measured on the postoperative x-rays. patients were divided into three groups: shortening group where the operated leg was more than 5mm shorter compared with the contralateral side, the restoration control group where the operated leg was within 5mm shortening and 9mm lengthening compared with the contralateral side, and the lengthening group where the operated leg became more than 9mm longer compared with the contralateral side.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Unilateral primary osteoarthritis (OA) treated with THA were considered for inclusion.

排除标准

  • Secondary OA.
  • Previous spinal, pelvic, or lower limb injuries or fractures.
  • Bilateral coxarthrosis.

结局指标

主要结局

WOMAC

时间窗: 12-15 months

次要结局

  • Visual analogue scale(12-15 months)
  • EQ-5D(12-15 months)

研究者

发起方
Sundsvall Hospital
申办方类型
Other
责任方
Sponsor

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