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临床试验/NCT02359266
NCT02359266已完成不适用

Clinical Trial Investigating the Role of Vitamin D in the Treatment of Depression in Patients With Chronic Liver Disease

Universität des Saarlandes2 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2011年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
111
试验地点
2
主要终点
Changes to depressive symptoms as assessed using the BDI-II score

研究概览

简要总结

This study evaluates the efficacy of vitamin D replacement therapy in reducing depressive symptoms in patients with chronic liver disease and vitamin D deficiency. Patients with normal vitamin D levels will be monitored as controls, and they will not receive any intervention.

详细描述

Patients with chronic liver diseases regularly suffer from vitamin D deficiency and depression. A recent meta-analysis reported an inverse correlation between depression and vitamin D levels. Indeed, vitamin D receptor is present and genomic and nongenomic vitamin D receptor-mediated signalling has been described in brain.

This intervention study investigates whether vitamin D therapy ameliorates depressive symptoms in chronic liver disease patients.

The investigators hypothesise that depressive symptoms will improve upon vitamin D replacement therapy.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • men and women
  • over 18 years of age
  • chronic liver disease

排除标准

  • severe hepatic encephalopathy (CFF <35 Hz)
  • Interferon treatment
  • hypercalcaemia (>2.7 mmol/l) or hypercalciuria (>8.0 mmol/d) with or without hyperparathyroidism (>65.0 pg/ml)
  • history of calcium-containing kidney stones
  • allergy or hypersensitivity to any of the supplement ingredients: peanuts, soy, gelatin
  • sarcoidosis
  • stage IV or V Chronic Kidney Disease
  • Pregnancy

结局指标

主要结局

Changes to depressive symptoms as assessed using the BDI-II score

时间窗: 3 and 6 months

次要结局

  • Changes to serum liver function tests, as assessed using standard clinical-chemical assays(3 and 6 months)
  • Changes to bone density, as assessed using Dexa scans(at 12 months)

研究者

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

Dr. Caroline Stokes

Dr

Universität des Saarlandes

研究点 (2)

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