跳至主要内容
临床试验/CTRI/2011/10/002086
CTRI/2011/10/002086招募中3 期

Antiproteinuric Effect of Oral Calcitriol in chronic Proteinuric Nephropathy:A randomized controlled trial.

ICMR0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
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

入选标准

  • 1.Normal blood pressure on stable doses of antihypertensive drugs for 1 month
  • 2.Estimated GFR 30 -90 ml/min/1.73 m2
  • 3.Children on corticosteroid should be on stable doses of corticosteroids for last 2 month

排除标准

  • Following children will be excluded from the study.
  • 1.Patients below 3 years of age
  • 2.Patients with estimated GFR 30 ml/min/1.73m2
  • 3.Patients with chronic liver disease or deranged transaminase levels (more than 2 times the normal)
  • 4.Patients with phosphorus levels 5.5 mg/dl, current hypercalcemia (serum calcium 10.5 mg/dl) or untreated primary hyperparathyroidism.
  • 5.Patients with hypercalciuria (24 h urinary calcium 4 mg/kg/d)
  • 6.Children residing outside 200km of the Delhi border.
  • 7.History of nephrolithiasis.
  • 8.Known malabsorption syndromes, e.g., celiac disease, active inflammatory bowel disease, etc.
  • 9.Treatment with vitamin D or any of its active metabolites in last 4 weeks
  • 10.Treatment with any drug which may interfere with vitamin D metabolism, e.g., phenobarbital, phenytoin.
  • 11.Patients with bilateral renal artery stenosis.
  • 12.Patients on immunosuppressive drugs such as cyclophosphamide, calcineurin inhibitors, azathioprine
  • 13.Steroid responsive nephrotic syndrome
  • 14.Patients on high dose (2 mg/kg/d prednisolone or equivalent) or intravenous corticosteroids

研究者

发起方
ICMR

相似试验