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临床试验/CTRI/2018/01/011225
CTRI/2018/01/011225进行中(未招募)4 期

A Randomized Controlled Trial to assess the effect of Vitamin D deficiency and supplementation on Bone Mineral Density in steroid sensitive nephrotic syndrome

Institute of Child Health1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2014年3月2日最近更新:

试验速览

阶段
4 期
状态
进行中(未招募)
入组人数
48
试验地点
1
主要终点
Bone mineral content and density

研究概览

简要总结

Steroid sensitive nephrotic syndrome (NS) is a common disease affecting Indian children. The majority of affected patients have multiple relapses over many years and require repeated and long term steroid courses. Steroid toxicities like osteoporosis have been well described in this condition and may cause long term morbidity, even after the NS has resolved. Reduction in bone mineralisation has been reported to occur early, within 2 to 3 months of steroid therapy. Unfortunately in the majority of patients steroid treatment cannot be avoided.

During NS episodes, there is loss of Vitamin D binding protein along with albumin in the urine. Patients have been shown to have low levels of 25 hydroxycholecalciferol in this condition. Correction of this associated hypovitaminosis D may improve bone health in this disease and reduce degree of osteoporosis.

In addition, low Vitamin D stores have been associated with inflammatory and infective conditions. Infections are the commonest precipitants of relapses in NS. Thus correction of hypovitaminosis D may reduce relapse rates in pediatric NS.

In this RCT, patients with NS relapse are recruited, and randomised into intervention and control groups. The intervention group receives Vitamin D and calcium supplements in the attempt to optimise serum 25hydroxycholecalciferol levels. Subsequently over a 6 month period, the changes in serum 25hydroxycholecalciferol, bone mineral density and bone mineral content as well as relapse rate is analysed and compared with the control group. Monitoring is performed for any adverse effects of Vitamin D therapy, such as hypercalcemia, hypercalciuria and nephrocalcinosis.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

年龄范围
2.00 Year(s) 至 14.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients with diagnosed steroid sensitive nephrotic syndrome 2.Age group: 2 to 14 years 3.Consecutive patients included during active NS episode 4.Urine protein more than 2+ for 3 consecutive days and urine protein creatinine ratio > 2 at recruitment.

排除标准

  • 1.Steroid Resistant nephrotic syndrome 2.Hospitalised patients 3.Any other acute or chronic illness 4.Patients with any bone deformities or symptoms related to the musculoskeletal system.

结局指标

主要结局

Bone mineral content and density

时间窗: at recruitment and post intervention after 6 months.

次要结局

  • Nephrotic Relapse rate(over 6 months)
  • serum 25 hydroxycholecalciferol levels(at recruitment and post intervention 6 weeks and 6 months)
  • Serum calcium and urinary calcium creatinine ratio(at recruitment and post intervention 6 weeks and 6 months)
  • renal ultrasound(after 6 months)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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