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临床试验/NCT05149729
NCT05149729Unknown不适用

Mid-Term Natural Course of Lower Extremity and Spine After Total Hip Arthroplasty in Patients With Crowe Type III-IV Hip Dysplasia

Bezmialem Vakif University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2021年2月10日最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
2
主要终点
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

研究概览

简要总结

Comparison of preoperative and postoperative mid-term course of patients with Crowe Type 3 and Type 4 hip dysplasia.

详细描述

Crowe type 3 and type 4 patients who underwent shortened hip replacement surgery will be followed up for 2 years.

Patients will be called for routine outpatient controls at the 2nd week, 6th week, 3rd month, 6th month, 12th month, 24th month.

Patients will be referred to the physical therapy specialist for abduction strengthening and pelvis tilt corrective exercises starting from the 6th week.

Scoliosis and orthoroentgenography x-rays will be taken at the last control of the patients.

HHS, WOMAC hip score and SF-12 score will be obtained from the patients. Scores, lower extremity and spine angles will be evaluated after the last examinations performed at 12 and 24 months.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

入选标准

  • Crowe type 3 and 4 patients over 18 years of age who had shortened hip replacement surgery

排除标准

  • Crowe type 1 or 2 patients over 18 years of age who had shortened hip replacement surgery
  • Patients who have previously operated on the contralateral hip
  • Patients who underwent shortened hip replacement for a reason other than developmental dysplasia of the hip

结局指标

主要结局

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

时间窗: The degree of improvement in Vomac score will be evaluated by looking at preoperative and postoperative 12th month Vomac scores.( 0-12th month )

The WOMAC score range, which indicates the clinical satisfaction of the patients, is between 0-100.

次要结局

未报告次要终点

研究者

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

Murat Sarikas

Orthopaedic surgeon

Bezmialem Vakif University

研究点 (2)

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