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临床试验/NL-OMON54781
NL-OMON54781招募中不适用

Protein turnover in the osteoarthritic knee; the impact of preoperative protein intake. - KneeT

niversiteit Maastricht0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Written informed consent
  • - Male and female patients scheduled for total knee arthroplasty
  • - BMI between 18.5-35 kg/m2
  • - Age >18 years
  • - Mentally competent, as judged by the treating physician
  • - Functioning gastrointestinal tract, eligible for oral protein supplementation

排除标准

  • - Corticosteroid injections less than 3 months prior to participation
  • - Any medications know to affect protein metabolism (i.e. systemic
  • corticosteroids or prescription strength acne medications)
  • - Lactose intolerance
  • - Insulineafhankelijke diabetes mellitus
  • - Alcohol abuse
  • - Rheumatoid arthritis
  • - Peripheral artery disease Fontaine III or IV
  • - COPD GOLD III or IV
  • - Pheynylketonuria
  • - Surgical intervention to the knee in the past four weeks
  • - Total parenteral nutrition at day of surgery
  • - Neoadjuvant chemotherapy or radiotherapy
  • - GFR <20 mL/min/1.73 m2
  • - Osteoarthritis of the knee secondary to septic arthritis, osteonecrosis,
  • fracture, OD, or malignant processes
  • - Collagen disorders, e.g. Marfan and Ehler-Danlos
  • - Any other medical condition that may interfere with the safety of the
  • subjects or the outcome parameters, in the investigators judgement
  • - Investigator*s uncertainty about the willingness or ability of the subject to
  • comply with the protocol instructions
  • - Participation in any other studies involving investigational or marketed
  • products concomitantly or within two weeks prior to entry into the study

研究者

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