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临床试验/DRKS00028082
DRKS00028082已完成不适用

Evaluation of the muscle perfusion of the M. gluteus medius after anterolateral minimally invasive versus conventional lateral Surgical access in total hip arthroplasty compared to healthy Opposite side using contrast-enhanced ultrasound (CEUS) - CEUS THA

Zentrum für Orthopädie, Unfallchirurgie und Paraplegiologie0 个研究点目标入组 80 人开始时间: 2022年2月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Adult patients who had a unilateral implantation 1-2 years ago have received a total hip replacement at the Heidelberg University Hospital and have a healthy, pain-free hip joint on the opposite side are included in the study.
  • Either the patients are included in their standard final examination Approx. 1 year postoperatively examined or contact is made via our Arthroplasty register and patient invitation for the study.

排除标准

  • Age under 18 years
  • - Inability to consent
  • - Known contrast media intolerance to SonoVue® or others ultrasound contrast media.
  • - Allergic reaction when given SonoVue®
  • - Lower extremity deformities
  • - Complaints or previous surgeries in the area of ??the contralateral hip joint
  • - Patients with known right-to-left shunt, severe pulmonary hypertension (pulmonary artery pressure > 90 mmHg), uncontrolled systemic hypertension or acute respiratory distress syndrome
  • - Pregnancy and breast feeding period.
  • - Lack of informed consent or
  • - refusal to participate.

研究者

发起方
Zentrum für Orthopädie, Unfallchirurgie und Paraplegiologie

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