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临床试验/NCT00609752
NCT00609752Unknown4 期

Adverse Effects of Glucocorticoid Therapy on Bone in Childhood Crohn's Disease

University Hospital Birmingham6 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2008年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
80
试验地点
6
主要终点
Bone mineral density change based on DXA measurement at 1 year

研究概览

简要总结

This study will compare two current first-line treatments for childhood Crohn's Disease, steroids versus a liquid diet, and determine the effects of these treatments on bone health, quality of life and treatment efficacy.

详细描述

Crohn's Disease is a very serious inflammatory gut disorder that often first presents in childhood. Once present, the underlying condition remains for life. It usually responds well to medical treatment which brings about a disease 'remission' but is inclined to become active again at intervals (relapses). When it is active, children are very unwell with reduced energy, loss of appetite and distressing abdominal symptoms (pain, diarrhea, etc.). Active disease can be treated in two very different ways - either with a 3-month course of steroids (tablets), or with a 6-week course of so called "liquid diet therapy (LDT)." With LDT, children receive all of their nutrition in liquid form. Both treatments have advantages and disadvantages. Both are quite effective, often controlling symptoms within days. Steroids may cause various side effects including thinning of bones (osteoporosis) with increased risk of fractures. LDT is somewhat challenging because normal (solid) foods are not allowed during the period of treatment. Both steroids and LDT are widely used - steroids predominately in the USA and LDT elsewhere. There is controversy as to which is best. This study aims to determine which should be preferred.

In this clinical study, children presenting with Crohn's disease will be randomly assigned to either steroid treatment or LDT and followed up for a period of one year. During that time the assigned treatment will be used for any episodes of active disease. We will study a total of 80 children attending the Paediatric Gastroenterology Units in Birmingham, Bristol, Liverpool, Oxford, Sheffield and St. George's Hospital in London. Various outcomes will be compared in the two groups. We will examine the recovery rates (success in bringing about remission) and the frequency of subsequent relapses. We will compare growth and physical development, because active Crohn's disease and possibly steroids may have adverse effects on these processes. A special focus of the study will be on the effect of the disease and its treatment on bone health. Using special blood and urine tests and bone scans we will compare bone growth and density in the two groups. Finally, it is crucially important that we consider the impact of the disease and its treatment on the young person on the basis of their own individual perspective. To do this we will compare the 'quality of life' of children in the two treatment groups, using a questionnaire specially designed to measure this aspect in young people with Crohn's disease.

This study will thus enable us to undertake a comprehensive comparison of the two major first-line treatments used in childhood Crohn's Disease. This is crucially important, and no such study has previously been undertaken

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
None

入排标准

年龄范围
7 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Active Crohn's Disease with PCDAI > 20
  • Aged 7 - 17 with possibility of 1 year follow-up

排除标准

  • Previous treatment for Crohn's Disease with liquid diet or glucocorticoid therapy
  • Isolated orofacial granulomatosis
  • Intravenous glucocorticoid therapy immediately indicated
  • Planned surgical intervention for CD

研究组 & 干预措施

1

Active Comparator

干预措施: prednisolone (Drug)

2

Active Comparator

干预措施: Alicalm (polymeric liquid formula) (Dietary Supplement)

结局指标

主要结局

Bone mineral density change based on DXA measurement at 1 year

时间窗: 12 months post-recruitment

次要结局

  • Proportion in remission(6 weeks)
  • Change in PCDAI, HAB and pHBS(6 weeks)
  • Quality of life throughout treatment period, using IMPACT III measurements(12 months)
  • Growth impairment(12 months)
  • Baseline urine 11B-HSD1 and bone formation(6 weeks)
  • Baseline urine 11B-HSD1 activity and change in bone mineral density(12 months)
  • Change in urine 11B-HSD1 activity and PCDAI in patients before and after treatment with LDT and CST(12 months)
  • Adherence to randomised therapy for relapses(12 months)
  • Adverse effects(12 months)

研究者

发起方
University Hospital Birmingham
申办方类型
Other

研究点 (6)

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