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临床试验/NL-OMON50642
NL-OMON50642已完成不适用

The effect of dietary interventions on endothelial glycocalyx dimensions and barrier function in South Asian patients with diabetic nephropathy. - Dietary interventions on glycocalyx dimensions in diabetic nephropathy.

eids Universitair Medisch Centrum0 个研究点目标入组 90 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
已完成
入组人数
90

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

  • 1. South Asian patient with diabetes mellitus type 2.
  • 2. Female or male, aged between 18 and 75 years.
  • 3. Body Mass Index *18.5.
  • 4. CKD-EPI >45 ml/min/1.73m² at baseline.
  • 5. Proven microalbuminuria defined as albumin/creatinine ratio *0.3 and <30
  • mg/mmol (single portion) or 3-300 mg albumin per day (24 hours urine
  • collection) in the last twelve months.
  • 6. Blood pressure of *180 mmHg with standard antihypertensive care.
  • 7. Treatment with hypoglycaemic drugs: metformin, sulphonylureas and/or
  • 8. Subject is willing to participate in the study, must be able to give
  • informed consent and the consent must be obtained prior to any study procedure.
  • 9. Patients must be able to adhere to the study visit schedule and protocol
  • requirements.
  • 10. If female and of child-bearing age, patients must be non-pregnant,
  • non-breastfeeding, and use adequate contraception.

排除标准

  • 1. Any concurrent illness, disability or clinically significant abnormality
  • that may, as judged by the investigator, affect the interpretation of clinical
  • efficacy or safety data or prevent the subject from safely completing the
  • assessments required by the protocol.
  • 2. Non-diabetic renal disease e.g. known polycystic kidney disease.
  • 3. Use of LMW heparin and/or immunosuppressive drugs.
  • 4. Significant food allergies for galactose, nuts, soy, tomato, corn, grape,
  • melon and artichoke, which would make the subject unable to consume the food
  • 5. Signs of active infection or autoimmune disease, requiring systemic
  • 6. A psychiatric, addictive or any disorder that compromises ability to give
  • truly informed consent for participation in this study.
  • 7. Malignancy (including lymphoproliferative disease) within the past 2-5 years
  • (except for squamous or basal cell carcinoma of the skin that has been treated
  • with no evidence of recurrence).
  • 8. Use of any other investigational drug.
  • 9. Patient has enrolled another clinical trial within last 4 weeks.

研究者

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