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临床试验/NCT06288451
NCT06288451进行中(未招募)2 期

DePTH: De-emphasize Parathyroid Hormone

University of Washington1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年3月11日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
90
试验地点
1
主要终点
Change in fibroblast growth factor-23

研究概览

简要总结

The De-emphasize Parathyroid Hormone (DePTH) Study is a 12-month pragmatic, randomized, parallel-group, active comparator, open-label, blinded end-point study of 90 patients with incident or prevalent secondary hyperparathyroidism and kidney failure treated with in-center hemodialysis. It tests the hypothesis that low fixed-dose oral calcitriol (intervention) will have more favorable effects on a comprehensive panel of biomarkers that assesses mineral metabolism, bone turnover, and serum calcification propensity, compared with variably-dosed intravenous activated vitamin D titrated to PTH targets (usual care).

详细描述

Because of the kidneys' major role in vitamin D metabolism, most patients with kidney failure on dialysis have biochemical abnormalities that include vitamin D deficiency and high levels of phosphate, fibroblast growth factor-23 (FGF-23), and parathyroid hormone (PTH). All of these abnormalities are associated with cardiovascular disease, bone disease, and death and are major reasons why nephrologists have treated patients on dialysis with activated vitamin D agents for over 30 years. Current guidelines, however, encourage nephrologists to use high doses of vitamin D in order to lower PTH levels to pre-specified treatment targets. This approach to treatment has not been proven to improve health and survival, and may be associated with several harms, including further increasing levels of FGF-23 (a major cardiovascular risk factor), increasing calcium levels, which may promote vascular calcification, low turnover bone disease, and interruptions in vitamin D treatments.

Administering a low, stable dose of vitamin D may be safer and more effective than the current standard of care. The De-emphasize PTH (DePTH) Study is a pragmatic randomized clinical trial of 90 patients on hemodialysis in Seattle, WA, USA that tests whether a low fixed-dose of oral calcitriol (the active form of vitamin D; study intervention) is more safe, effective, and feasible compared with the current usual care. Participants will be recruited at their hemodialysis treatment centers and randomized in a 1:1 ratio to one of these two treatment strategies and followed over 12 months. Participants randomized to the study intervention will receive a fixed dose of calcitriol 0.5 mcg three times a week at their dialysis treatment sessions regardless of PTH level over the ensuing 12 months. Participants randomized to usual care will maintain the existing approach to treating abnormal mineral metabolism using vitamin D doses titrated to monthly to quarterly measurements of PTH. The outcomes for this trial are a panel of blood-based measurements of bone and vascular health that will be drawn at the same time as the blood work done monthly as part of routine dialysis care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The outcomes assessors are blinded to the assigned interventions.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age >=18 years
  • Kidney failure treated with in-center hemodialysis
  • PTH >=150 pg/mL x 2 consecutive measures at least 1 month apart or active IV activated vitamin D treatment using the NKC protocol

排除标准

  • History of parathyroidectomy or calciphylaxis
  • Severe secondary hyperparathyroidism (PTH >=600 pg/mL x 2 consecutive measures at least 1 month apart despite paricalcitol >=10 mcg 3x/week or doxercalciferol >=5 mcg 3x/week or cinacalcet >30 mg/d)
  • Calcium >9.8 mg/dL
  • Phosphate >9 mg/dL
  • Cholestyramine, phenytoin/phenobarbital, or ketoconazole use
  • Breast-feeding mothers
  • Inability to provide informed consent and no legally authorized representative

研究组 & 干预措施

Low dose oral calcitriol

Experimental

干预措施: Oral calcitriol with cinacalcet rescue (Drug)

Usual care

Active Comparator

干预措施: IV activated vitamin D (Drug)

结局指标

主要结局

Change in fibroblast growth factor-23

时间窗: 12 months

Change in fibroblast growth factor-23

次要结局

  • Change in serum calcium(12 months)
  • Change in serum phosphate(12 months)
  • Change in serum bone-specific alkaline phosphatase(12 months)
  • Change in serum parathyroid hormone(12 months)
  • Change in T50 test of serum calcification propensity(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Simon Hsu, MD, MS

Assistant Professor

University of Washington

研究点 (1)

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